Search Results - "Grinas, Laurent"

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    Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping by Hillaire, D, Leclerc, A, Fauré, S, Topaloglu, H, Chiannilkulchaï, N, Guicheney, P, Grinas, L, Legos, P, Philpot, J, Evangelista, T

    Published in Human molecular genetics (1994)
    “…Congenital muscular dystrophies (CMD) are autosomal recessive, heterogeneous disorders. The commonest forms are the Fukuyama CMD (FCMD), associated with mental…”
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    Journal Article