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Nosel POMT2 mutations associated with a marked reduction of POMT activity causing congenital muscular dystrophy with mental retardation and microcephaly

Bibliographic reference Yanagisawa, A. ; Van den Bergh, Peter ; Bouchet, C. ; Manya, H. ; Quijano-Roy, S. ; et. al. Nosel POMT2 mutations associated with a marked reduction of POMT activity causing congenital muscular dystrophy with mental retardation and microcephaly.12th International Congress of the World-Muscle-Society (Giardini Naxos (Italy), Oct 17-20, 2007). In: Neuromuscular Disorders, Vol. 17, no. 9-10, p. 870-870 (2007)
Permanent URL http://hdl.handle.net/2078.1/59489