Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A. (Q31158469)

29 June 2017

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A. (English)

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29 June 2017

Matsunami N

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29 June 2017

Smith B

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Ballard L

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29 June 2017

Lensch MW

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29 June 2017

Robertson M

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Albertsen H

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29 June 2017

Hanemann CO

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Müller HW

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Bird TD

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White R

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language of work or name

English

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publication date

1 June 1992

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29 June 2017

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29 June 2017

1

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176-179

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https://scigraph.springernature.com/pub.10.1038/ng0692-176

29 June 2017

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cites work

Trembler mouse carries a point mutation in a myelin gene

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https://api.crossref.org/works/10.1038%2FNG0692-176

A growth arrest-specific (gas) gene codes for a membrane protein

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0692-176

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

Genetic aspects of hereditary motor and sensory neuropathy (types I and II)

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

Two new mutants, ‘trembler’ and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

Abnormal myelination in transplanted Trembler mouse Schwann cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

Long lives for homozygous trembler mutant mice despite virtual absence of peripheral nerve myelin

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

Status of the linkage map of the mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

The physical map of Mus musculus chromosome 11 reveals evolutionary relationships with different syntenic groups of genes in Homo sapiens

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

A myelin protein is encoded by the homologue of a growth arrest-specific gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-176

7 January 2021

Identifiers

DOI

10.1038/NG0692-176

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Dimensions Publication ID

29 June 2017

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