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A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.

Arthrogryposis multiplex congenita (AMC) is a heterogeneous-symptom complex characterized by joint contractures at birth that involve more than one part of the body. We performed a genetic-linkage study of one large Israeli-Arab inbred kindred showing autosomal recessive inheritance of AMC neuropath...

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Autores principales: Shohat, M, Lotan, R, Magal, N, Shohat, T, Fischel-Ghodsian, N, Rotter, J I, Jaber, L
Formato: Artigo
Lenguaje:Inglês
Publicado: 1997
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1716024/
https://ncbi.nlm.nih.gov/pubmed/9345093
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