Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian families. (Q42638792)

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29 December 2019

title

Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian families (English)

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29 December 2019

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9

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29 December 2019

Tsukasa Saito

1

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29 December 2019

author name string

Yoshinobu Amakusa

2

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29 December 2019

Takashi Kimura

3

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29 December 2019

Osamu Yahara

4

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29 December 2019

Hitoshi Aizawa

5

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29 December 2019

Yoshio Ikeda

6

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29 December 2019

John W Day

7

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29 December 2019

Laura P W Ranum

8

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Tohru Matsuura

10

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language of work or name

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5 December 2007

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29 December 2019

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volume

9

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issue

1

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page(s)

61-63

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An improved method for Southern DNA and Northern RNA blotting using a Mupid-2 Mini-Gel electrophoresis unit

29 December 2019

cites work

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12 December 2020

Myotonic dystrophy type 2: human founder haplotype and evolutionary conservation of the repeat tract

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12 December 2020

Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?

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12 December 2020

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

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12 December 2020

Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies. 3rd Workshop, 14-16 February 2003, Naarden, The Netherlands

1 reference

12 December 2020

Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts

1 reference

12 December 2020

Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect

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12 December 2020

140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management

1 reference

12 December 2020

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

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12 December 2020

Myotonic dystrophy with no trinucleotide repeat expansion

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12 December 2020

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum

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12 December 2020

10.1007/S10048-007-0110-4

Identifiers

DOI

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29 December 2019

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