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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]
- 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
- Subjects :
- Genetics
medicine.medical_specialty
MCARDLE DISEASE
Endocrinology, Diabetes and Metabolism
media_common.quotation_subject
Bachelor
Biochemistry
Endocrinology
Geography
Myophosphorylase
Family medicine
medicine
In patient
University medical
Dominant inheritance
Anatomical science
High Street
Molecular Biology
media_common
Subjects
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