Five New Cases of Syndromic Intellectual Disability Due to KAT6A Mutations: Widening the Molecular and Clinical Spectrum
Orphanet Journal of Rare Diseases - United Kingdom
doi 10.1186/s13023-020-1317-9
Full Text
Open PDFAbstract
Available in full text
Date
February 10, 2020
Authors
Publisher
Springer Science and Business Media LLC