Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity.

Tuberous sclerosis (TSC) is an autosomal dominant disorder with both neurological and cutaneous manifestations often resulting in significant disability. Although it has been studied clinically and biochemically for many years, the underlying pathophysiology remains unknown. Genetic linkage analysis...

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Detalhes bibliográficos
Main Authors: Haines, J L, Short, M P, Kwiatkowski, D J, Jewell, A, Andermann, E, Bejjani, B, Yang, C H, Gusella, J F, Amos, J A
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683174/
https://ncbi.nlm.nih.gov/pubmed/1897523
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