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Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita
Ekhilevitch, N., Kurolap, A., Oz-Levi, D., Mory, A., Hershkovitz, T., Ast, G., Mandel, H., Baris, H.N.Volume:
90
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12707
Date:
July, 2016
File:
PDF, 656 KB
english, 2016