Minimally symptomatic mcardle disease, expanding the genotype-phenotype spectrum
Author:
Affiliation:
1. Department of Biochemical Genetics; The Cyprus Institute of Neurology and Genetics; Nicosia Cyprus
2. Neurology Clinics A & C; The Cyprus Institute of Neurology and Genetics; P.O. Box 23462 1683 Nicosia Cyprus
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
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