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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Hauptverfasser: Haines, J L, Short, M P, Kwiatkowski, D J, Jewell, A, Andermann, E, Bejjani, B, Yang, C H, Gusella, J F, Amos, J A
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1991
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683174/
https://ncbi.nlm.nih.gov/pubmed/1897523
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