Knock-in mice for the R50X mutation in the PYGM gene present with McArdle disease-Reference-Cited by-同舟云学术

Knock-in mice for the R50X mutation in the PYGM gene present with McArdle disease

Published:2012-06-12 Issue:7 Volume:135 Page:2048-2057
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Nogales-Gadea Gisela,Pinós Tomàs,Lucia Alejandro,Arenas Joaquín,Camara Yolanda,Brull Astrid,de Luna Noemí,Martín Miguel A.,Garcia-Arumí Elena,Martí Ramon,Andreu Antoni L.

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/135/7/2048/13801110/aws141.pdf

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4. Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: identification of 10 new mutations. Absence of genotype-phenotype correlation;Aquaron;Neuromuscul Disord,2007

5. The glucagon-like peptide-1 receptor regulates endogenous glucose production and muscle glucose uptake independent of its incretin action;Ayala;Endocrinology,2009

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