Whole exome sequencing identified FAM149A as a plausible causative gene for congenital hereditary endothelial dystrophy, affecting Nrf2-Antioxidant signaling upon oxidative stress-Reference-Cited by-同舟云学术

Whole exome sequencing identified FAM149A as a plausible causative gene for congenital hereditary endothelial dystrophy, affecting Nrf2-Antioxidant signaling upon oxidative stress

Published:2021-09 Issue: Volume:173 Page:117-124
ISSN:0891-5849
Container-title:Free Radical Biology and Medicine
language:en
Short-container-title:Free Radical Biology and Medicine

Author:

Zhang Jing,Dai Yiqin,Wu Dan,Li Yue,Xu Jianjiang^ORCID

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Physiology (medical),Biochemistry

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4. Outcomes of penetrating keratoplasty in congenital hereditary endothelial dystrophy;AlArrayedh;Br. J. Ophthalmol.,2018

5. Penetrating keratoplasty in young children with congenital hereditary endothelial dystrophy;Javadi;Cornea,2003

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