Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder
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Genetics in medicine - ISSN 1530-0366-24:7 (2022) p. 1583-1591
A human importin-β-related disorder : syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8
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The American journal of human genetics - ISSN 0002-9297-108:6 (2021) p. 1115-1125