TRAPPC9-related neurodevelopmental disorder: Report of a homozygous deletion in TRAPPC9 due to paternal uniparental isodisomy.

American journal of medical genetics. Part A

2022

https://researcherprofiles.org/profile/358259746

36574751

Penon-Portmann M, Hodoglugil U, Arun P W, Yip T, Slavotinek A, Tenney JL