P.P.1 01 Congenital muscular dystrophy with mental retradation due to a homozygous protein-o-mannosyltransferase 2 (POMT2) mutation: A case report
P.Y.K. Van den Bergh, C. Bouchet, S. Maugenre, A. Yanagisawa, G. Cosnard, F. Leturcq, N. Deburgrave, N. Séta, P. GuicheneyVolume:
16
Year:
2006
Language:
english
DOI:
10.1016/j.nmd.2006.05.070
File:
PDF, 49 KB
english, 2006