Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: An animal model of human Brody disease-Reference-Cited by-同舟云学术

Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: An animal model of human Brody disease

Published:2008-12 Issue:6 Volume:92 Page:474-477
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Drögemüller Cord,Drögemüller Michaela,Leeb Tosso,Mascarello Francesco,Testoni Stefania,Rossi Marco,Gentile Arcangelo,Damiani Ernesto,Sacchetto Roberta

Publisher

Elsevier BV

Subject

Genetics

Reference17 articles.

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3. Muscle contracture induced by exercise: a syndrome attributable to decreased relaxing factor;Brody;New Eng. J. Med.,1969

4. Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ATPase, are associated with Brody disease;Odermatt;Nat. Genet.,1996

5. Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease;Odermatt;Genomics,1997

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