Zobrazeno 1 - 2 of 2 pro vyhledávání: '"Haniyeh POURKALHOR"'
1
Akademický článek
A Homozygote Mutation in S-Antigen Visual Arrestin SAG Gene in an Iranian Patient with Oguchi Type One: A Case Report
Autor: Hajar ARYAN, Atekeh BAHADORI, Dariush D. FARHUD, Marjan ZARIF YEGANEH, Haniyeh POURKALHOR
Publikováno v: Iranian Journal of Public Health, Vol 49, Iss 5 (2020)
Oguchi disease is a rare autosomal recessive form of congenital stationary night blindness (CSNB) characterized by specific features such as golden-brown discoloration of the fundus called Mizuo-Nakamura phenomenon which is distinguishable by fundosc
Externí odkaz: https://doaj.org/article/7ead0c2fa3f14610a8359ace909f1a7a
Zobrazit plný text záznamu
2
A Homozygote Mutation in S-Antigen Visual Arrestin SAG Gene in an Iranian Patient with Oguchi Type One: A Case Report
Autor: Marjan Zarif Yeganeh, Dariush D. Farhud, Haniyeh Pourkalhor, Hajar Aryan, Atekeh Bahadori
Publikováno v: Iranian Journal of Public Health, Vol 49, Iss 5 (2020)
Iranian Journal of Public Health
Oguchi disease is a rare autosomal recessive form of congenital stationary night blindness (CSNB) characterized by specific features such as golden-brown discoloration of the fundus called Mizuo-Nakamura phenomenon which is distinguishable by fundosc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e5306a1b30d86907fbb80ca3e50e4f3
https://ijph.tums.ac.ir/index.php/ijph/article/view/14458
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje