Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population

IMPORTANCE: The c.1102C>T, p.(Gln368Ter) variant in the myocilin (MYOC) gene is a known risk allele for glaucoma. It is the most common MYOC risk variant for glaucoma among individuals of European ancestry, and its prevalence is highest in Finland. Furthermore, exfoliation syndrome has high preva...

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Detalhes bibliográficos
Publicado no:JAMA Ophthalmol
Main Authors: Liuska, Perttu J., Lemmelä, Susanna, Havulinna, Aki S., Kaarniranta, Kai, Uusitalo, Hannu, Laivuori, Hannele, Kiiskinen, Tuomo, Daly, Mark J., Palotie, Aarno, Turunen, Joni A.
Formato: Artigo
Idioma:Inglês
Publicado em: American Medical Association 2021
Assuntos:
Original Investigation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8176385/
https://ncbi.nlm.nih.gov/pubmed/34081096
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamaophthalmol.2021.1610
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