A rare optineurin mutation in an Indian family with coexistence of JOAG and PCG.

Yadav, Manoj; Yadav, Anshu; Bhardwaj, Aarti; Dhull, Chand Singh; Sachdeva, Sumit; Yadav, Ritu; Tanwar, Mukesh

Yadav, Manoj; Yadav, Anshu; Bhardwaj, Aarti; Dhull, Chand Singh; Sachdeva, Sumit; Yadav, Ritu; Tanwar, Mukesh.

Afiliação

Yadav M; Department of Genetics, Maharshi Dayanand University, Rohtak, Harayana, India.
Yadav A; Department of Genetics, Maharshi Dayanand University, Rohtak, Harayana, India.
Bhardwaj A; Department of Genetics, Maharshi Dayanand University, Rohtak, Harayana, India.
Dhull CS; Regional Institute of Ophthalmology, Pt. B.D. Sharma University of Health Sciences, Rohtak, Haryana, India.
Sachdeva S; Regional Institute of Ophthalmology, Pt. B.D. Sharma University of Health Sciences, Rohtak, Haryana, India.
Yadav R; Department of Genetics, Maharshi Dayanand University, Rohtak, Harayana, India.
Tanwar M; Department of Genetics, Maharshi Dayanand University, Rohtak, Harayana, India.

Indian J Ophthalmol ; 71(8): 3016-3023, 2023 08.

Article em En | MEDLINE | ID: mdl-37530275

Assuntos

Glaucoma de Ângulo Aberto; Glaucoma; Humanos; Mutação; Testes Genéticos; Linhagem; Proteínas do Olho/genética; Proteínas do Olho/metabolismo; Análise Mutacional de DNA

Palavras-chave

Cytochrome P450; juvenile open-angle glaucoma; myocilin; optineurin; primary congenital glaucoma

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glaucoma / Glaucoma de Ângulo Aberto Limite: Humans Idioma: En Revista: Indian J Ophthalmol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Índia

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google