Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA
Year: 1998
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/7.3.471
Institution: Oregon Health & Science University
Language: English
Topic: Connexins and lens biology
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2115644880