(Q42638792)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18057971%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

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

1 reference

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29 December 2019

1 reference

9

1 reference

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29 December 2019

Tsukasa Saito

1

1 reference

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29 December 2019

author name string

Yoshinobu Amakusa

2

1 reference

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29 December 2019

Takashi Kimura

3

1 reference

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29 December 2019

Osamu Yahara

4

1 reference

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29 December 2019

Hitoshi Aizawa

5

1 reference

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29 December 2019

Yoshio Ikeda

6

1 reference

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29 December 2019

John W Day

7

1 reference

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29 December 2019

Laura P W Ranum

8

1 reference

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29 December 2019

Tohru Matsuura

10

1 reference

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29 December 2019

language of work or name

1 reference

5 December 2007

1 reference

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29 December 2019

1 reference

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29 December 2019

volume

9

1 reference

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29 December 2019

issue

1

1 reference

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29 December 2019

page(s)

61-63

1 reference

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https://scigraph.springernature.com/pub.10.1007/s10048-007-0110-4

29 December 2019

exact match

0 references

cites work

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

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.

1 reference

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

1 reference

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

1 reference

12 December 2020

Myotonic dystrophy with no trinucleotide repeat expansion

1 reference

12 December 2020

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum

1 reference

12 December 2020

10.1007/S10048-007-0110-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18057971%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference