Evidence that a locus for familial high myopia maps to chromosome 18p.

Myopia, or nearsightedness, is the most common human eye disorder. A genomewide screen was conducted to map the gene(s) associated with high, early-onset, autosomal dominant myopia. Eight families that each included two or more individuals with >=-6.00 diopters (D) myopia, in two or more successi...

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Detalhes bibliográficos
Main Authors: Young, T L, Ronan, S M, Drahozal, L A, Wildenberg, S C, Alvear, A B, Oetting, W S, Atwood, L D, Wilkin, D J, King, R A
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377231/
https://ncbi.nlm.nih.gov/pubmed/9634508
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