(Q54266671)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26060040%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

title

Clinical applications of next-generation sequencing-based gene panel in patients with muscular dystrophy: Korean experience (English)

1 reference

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16 February 2020

1 reference

1

1 reference

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16 February 2020

author name string

A Cho

2

1 reference

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16 February 2020

H W Park

3

1 reference

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16 February 2020

S H Seo

4

1 reference

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16 February 2020

B C Lim

5

1 reference

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16 February 2020

D Seol

6

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16 February 2020

S I Cho

7

1 reference

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16 February 2020

S S Park

8

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16 February 2020

J H Chae

9

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16 February 2020

publication date

29 June 2015

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16 February 2020

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16 February 2020

volume

89

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16 February 2020

issue

4

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16 February 2020

page(s)

484-488

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Limb-girdle muscular dystrophy

16 February 2020

cites work

1 reference

Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes

21 January 2018

1 reference

Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan.

21 January 2018

1 reference

Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients

21 January 2018

1 reference

Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathy.

21 January 2018

1 reference

Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2B.

21 January 2018

1 reference

Analysis of the DYSF mutational spectrum in a large cohort of patients

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12621

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26060040%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

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