Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathy (Q28139741)

scientific article (publication date: July 1999)

Language	Label	Description	Also known as
English	Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathy	scientific article (publication date: July 1999)

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scholarly article

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title

Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathy (English)

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1 reference

L Merlini

1

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M Villanova

series ordinal

2

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P Sabatelli

series ordinal

3

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A Malandrini

series ordinal

4

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N M Maraldi

series ordinal

5

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language of work or name

English

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publication date

July 1999

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published in

Neuromuscular Disorders

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volume

9

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issue

5

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page(s)

326-9

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cites work

Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees

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7 January 2021

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Further investigations on benign myopathy with autosomal dominant inheritance

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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Bethlem myopathy: Early-onset benign autosomal dominant myopathy with contractures. Description of two new families

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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Early-onset benign autosomal dominant limb-girdle myopathy with contractures (Bethlem myopathy)

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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Type VI collagen anchors endothelial basement membranes by interacting with type IV collagen

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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Expression of laminin subunits in congenital muscular dystrophy

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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Abnormal localization of laminin subunits in muscular dystrophies

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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Abnormal expression of laminin beta 1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

based on heuristic

inferred from DOI database lookup

Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1?

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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inferred from DOI database lookup

Basement Membrane Proteins: Structure, Assembly, and Cellular Interactions

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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inferred from DOI database lookup

Basal lamina assembly

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900022-X

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7 January 2021

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Identifiers

DOI

10.1016/S0960-8966(99)00022-X

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PubMed publication ID

10407855

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Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathy (Q28139741)

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Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathy (Q28139741)

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