A Novel AAAS Gene Mutation in Allgrove Syndrome: Case Report and Genetic Insights from a Chinese Xinjiang Girl.
Year: 2025
Type: article
Study design: Case Report
Source: PubMed
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4414340999
FWCI:
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