Missense mutations in MIP underlie autosomal dominant ‘polymorphic’ and lamellar cataracts linked to 12q
Year: 2000
Type: article
Source: Nature Genetics
DOI: 10.1038/75538
Institutions: Moorfields Eye Hospital, Addenbrooke's Hospital
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2008726342
