PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.

P. Guicheney,N. Vignier,Xu Zhang,Yi He,C. Cruaud,V. Frey,A. Helbling-Leclerc,P. Richard,B. Estournet,L. Merlini,H. Topaloğlu,M. Mora,J. Harpey,C. Haenggeli,A. Barois,B. Hainque,K. Schwartz,F. Tomé,M. Fardeau,K. Tryggvason

Published 1998 in Journal of Medical Genetics

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