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Medical genetics: advances in brief: Myophosphorylase deficiency: an unusually severe form with myoglobinuria
Clayton-Smith, J.Volume:
32
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.32.1.76-a
Date:
January, 1995
File:
PDF, 267 KB
english, 1995