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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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
Format: Artigo
Jezik:Inglês
Izdano: 1991
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683174/
https://ncbi.nlm.nih.gov/pubmed/1897523
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