(Q47242771)

English

Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations

scientific article published in July 2004

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scholarly article

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations (English)

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

1 reference

based on heuristic

inferred from title

nemaline myopathy

1 reference

based on heuristic

inferred from title

8

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

12

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Charles R Midgett

object named as

Charles Midgett

3

0 references

object named as

Nigel G Laing

11

0 references

Susan T. Iannaccone

9

object named as

Susan T Iannaccone

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

author name string

Pankaj B Agrawal

1

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Corinne D Strickland

2

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Ana Morales

4

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Daniel E Newburger

5

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Melisa A Poulos

6

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Kinga K Tomczak

7

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Tom O Crawford

10

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

publication date

1 July 2004

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Annals of Neurology

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

56

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

86-96

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

1

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

Clinical course correlates poorly with muscle pathology in nemaline myopathy.

1 reference

https://api.crossref.org/works/10.1002%2FANA.20157

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.20157

21 January 2018

Distinct light microscopic changes in human immunodeficiency virus-associated nemaline myopathy

1 reference

https://api.crossref.org/works/10.1002%2FANA.20157

21 January 2018

Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome

1 reference

https://api.crossref.org/works/10.1002%2FANA.20157

21 January 2018

Identifiers

10.1002/ANA.20157

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

1 reference

Europe PubMed Central

12 January 2018

http://europepmc.org/abstract/MED/15236405

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