(Q36193679)

12 August 2017

1 reference

title

When contractile proteins go bad: the sarcomere and skeletal muscle disease (English)

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12 August 2017

Nigel G Laing

1

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12 August 2017

Kristen J Nowak

series ordinal

2

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12 August 2017

language of work or name

English

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publication date

1 August 2005

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12 August 2017

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12 August 2017

volume

27

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12 August 2017

issue

8

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12 August 2017

page(s)

809-822

1 reference

Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

12 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FBIES.20269

Mutations in myotilin cause myofibrillar myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBIES.20269

Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBIES.20269

Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBIES.20269

Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBIES.20269

Clinical course correlates poorly with muscle pathology in nemaline myopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBIES.20269

21 January 2018

Identifiers

DOI

10.1002/BIES.20269

1 reference

12 August 2017

1 reference