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Marfan syndrome: No evidence for heterogeneity in different populations, and more precise mapping of the gene

Marfan syndrome is a dominantly inherited connective tissue disorder with manifestations in the cardiovascular, ocular, and skeletal systems. The diagnosis is hampered by both high variability in the phenotypic expression and late manifestation of symptoms. The cause of Marfan syndrome remains unkno...

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Detalhes bibliográficos
Main Authors: Kainulainen, Katariina, Steinmann, Beat, Collins, Francis, Dietz, Harry C., Francomano, Clair A., Child, Anne, Kilpatrick, Michael W., Brock, David J. H., Keston, Marion, Pyeritz, Reed E., Peltonen, Leena
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683142/
https://ncbi.nlm.nih.gov/pubmed/1882844
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