EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome
Year: 2000
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/78085
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W1505761263
