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Corrigendum to 'Six novel mutations in the myophosphorylase gene in patients with McArdle disease and a family with pseudo-dominant inheritance pattern' [Mol. Genet. Metab. 104 (2011) 587–591]

Authors :
Y. Wu
J.L. Weber
Georgirene D. Vladutiu
Mark A. Tarnopolsky
Source :
Molecular Genetics and Metabolism. 111:539
Publication Year :
2014
Publisher :
Elsevier BV, 2014.

Abstract

a Department of Pediatrics, McMaster University Medical Centre, 1200 Main Street West, Hamilton, Ontario L8N 3Z5, Canada b Bachelor of Health Sciences (Honours) Program, Faculty of Health Sciences, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4K1, Canada c Prevention Genetics, 3700 Downwind Drive, Marshfield, WI 54449, USA d Department of Pediatrics, The University at Buffalo, 100 High Street, Buffalo, NY 14203, USA e Department of Neurology, The University at Buffalo, 100 High Street, Buffalo, NY 14203, USA f Department of Pathology and Anatomical Sciences, The University at Buffalo, 100 High Street, Buffalo, NY 14203, USA g Department of Medicine (Neurology and Rehabilitation), McMaster University Medical Centre, 1200 Main Street West, Hamilton, Ontario L8N 3Z5, Canada

Details

ISSN :
10967192
Volume :
111
Database :
OpenAIRE
Journal :
Molecular Genetics and Metabolism
Accession number :
edsair.doi...........ee72ea63c8d1119d41a83696e304064a
Full Text :
https://doi.org/10.1016/j.ymgme.2014.02.006