P.P.4 08 Pediatric patients homozygous for the c.826C > A missense mutation in the FKRP gene: Experience from a Norwegian pediatric service
M. Rasmussen, C. Jonsrud, O.C. Borota, S. Lindal, N. Breivik, M. Mork, K. SkullerudVolume:
16
Year:
2006
Language:
english
DOI:
10.1016/j.nmd.2006.05.125
File:
PDF, 46 KB
english, 2006