Investigation of mutational spectrum in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma.

Zahid, Tazeen; Khan, Muhammad Umer; Zulfiqar, Aymn; Jawad, Fatima; Saleem, Anosh; Khan, Ahmad Raza

Zahid, Tazeen; Khan, Muhammad Umer; Zulfiqar, Aymn; Jawad, Fatima; Saleem, Anosh; Khan, Ahmad Raza.

Afiliação

Zahid T; Tazeen Zahid DMLS, MPhil Scholar., Institute of Molecular Biology and Biotechnology, The University of Lahore, Lahore, Pakistan.
Khan MU; Muhammad Umer Khan, MPhil, PhD., Institute of Molecular Biology and Biotechnology, The University of Lahore, Lahore, Pakistan.
Zulfiqar A; Aymn Zulfiqar, DMLS., University Institute of Medical Laboratory Technology, Faculty of Allied Health Sciences, The University of Lahore, Lahore, Pakistan.
Jawad F; Fatima Jawad, DMLS., University Institute of Medical Laboratory Technology, Faculty of Allied Health Sciences, The University of Lahore, Lahore, Pakistan.
Saleem A; Anosh Saleem, DMLS., University Institute of Medical Laboratory Technology, Faculty of Allied Health Sciences, The University of Lahore, Lahore, Pakistan.
Khan AR; Ahmad Raza Khan, DMLS., University Institute of Medical Laboratory Technology, Faculty of Allied Health Sciences, The University of Lahore, Lahore, Pakistan.

Pak J Med Sci ; 39(2): 409-416, 2023.

Article em En | MEDLINE | ID: mdl-36950438

Palavras-chave

Consanguinity; Cytochrome P450; Intraocular pressure; Mutation; Primary congenital glaucoma

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Aspecto: Ethics Idioma: En Revista: Pak J Med Sci Ano de publicação: 2023 Tipo de documento: Article

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