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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Dades bibliogràfiques
Publicat a:JAMA Ophthalmol
Autors principals: Liuska, Perttu J., Lemmelä, Susanna, Havulinna, Aki S., Kaarniranta, Kai, Uusitalo, Hannu, Laivuori, Hannele, Kiiskinen, Tuomo, Daly, Mark J., Palotie, Aarno, Turunen, Joni A.
Format: Artigo
Idioma:Inglês
Publicat: American Medical Association 2021
Matèries:
Original Investigation
Accés en línia: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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