Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.

Familial lattice corneal dystrophy type I (LCD1) is a localized form of inherited amyloidosis limited to the corneal stroma. Recently the Finnish form of hereditary amyloidosis with lattice corneal dystrophy has been shown to be due to a mutation in the gelsolin gene (G654----A; Asp187----Asn). In t...

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Detalhes bibliográficos
Main Authors: Wiens, A, Marles, S, Safneck, J, Kwiatkowski, D J, Maury, C P, Zelinski, T, Philipps, S, Ekins, M B, Greenberg, C R
Formato: Artigo
Idioma:Inglês
Publicado em: 1992
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682887/
https://ncbi.nlm.nih.gov/pubmed/1319113
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