학술논문
Multimorbidity due to novel pathogenic variants in the WFS1/RP1/NOD2 genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British family
Document Type
Article
Author
Source
In: BMJ Open Ophthalmology . (BMJ Open Ophthalmology, 14 July 2023, 8(1))
Subject
Language
English
ISSN
23973269