(Q30168391)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257470%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

title

Abnormalities in the expression of nebulin in chromosome-2 linked nemaline myopathy (English)

1 reference

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5 November 2019

2

1 reference

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5 November 2019

Heinz Jungbluth

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257470%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

author name string

C A Sewry

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257470%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

K Pelin

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257470%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

C Wallgren-Pettersson

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257470%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

S Labeit

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257470%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

A Manzur

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257470%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

F Muntoni

8

1 reference

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5 November 2019

publication date

1 March 2001

1 reference

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5 November 2019

published in

Neuromuscular Disorders

1 reference

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5 November 2019

volume

11

1 reference

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5 November 2019

issue

2

1 reference

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5 November 2019

page(s)

146-153

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257470%20AND%20SRC:MED&resulttype=core&format=json

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy

5 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900172-3

7 January 2021

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900172-3

7 January 2021

Experimental regeneration in canine muscular dystrophy--2. Expression of myosin heavy chain isoforms

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900172-3

7 January 2021

Deficiency of a skeletal muscle isoform of α-actinin (α-actinin-3) in merosin-positive congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900172-3

7 January 2021

Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900172-3

7 January 2021

The hazards of home oxygen therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900172-3

7 January 2021

The role of immunocytochemistry in congenital myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900172-3

7 January 2021

10.1016/S0960-8966(00)00172-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257470%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference