(Q55032944)

English

A common nonsense mutation results in alpha-actinin-3 deficiency in the general population.

scientific article published in April 1999

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

A common nonsense mutation results in alpha-actinin-3 deficiency in the general population. (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

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1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

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1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

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1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

author name string

Yang N

2

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

Wattanasirichaigoon D

3

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

Mills M

4

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

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1 April 1999

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

Nature Genetics

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

353-354

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

The structure and function of alpha-actinin

1 reference

https://api.crossref.org/works/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy

1 reference

https://api.crossref.org/works/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

Progressive depletion of fast alpha-actinin-positive muscle fibers in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

Testing for linkage disequilibrium in genotypic data using the Expectation-Maximization algorithm

1 reference

https://api.crossref.org/works/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

Evolutionary origins and maintenance of redundant gene expression during metazoan development

1 reference

https://api.crossref.org/works/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

Human skeletal muscle-specific alpha-actinin-2 and -3 isoforms form homodimers and heterodimers in vitro and in vivo

1 reference

https://api.crossref.org/works/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

Further analysis of the role of spectrin repeat motifs in alpha-actinin dimer formation.

1 reference

https://api.crossref.org/works/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

Unbiased estimation of the rates of synonymous and nonsynonymous substitution

1 reference

https://api.crossref.org/works/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences

1 reference

https://api.crossref.org/works/10.1038%2F7675

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/10192379

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