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A mutation in the RIEG1 gene associated with Peters' anomaly

Mutations within the RIEG1 homeobox gene on chromosome 4q25 have previously been reported in association with Rieger syndrome. We report a 3' splice site mutation within the 3rd intron of the RIEG1 gene which is associated with unilateral Peters' anomaly. The mutation is a single base subs...

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Detalhes bibliográficos
Main Authors: Doward, W, Perveen, R, Lloyd, I, Ridgway, A, Wilson, L, Black, G
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 1999
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734311/
https://ncbi.nlm.nih.gov/pubmed/10051017
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