A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

(The American Journal of Human Genetics 111, 96 –118, January 4, 2024)

Source: The American Journal of Human Genetics - March 19, 2024 Category: Genetics & Stem Cells Authors: Maimuna S. Paul, Sydney L. Michener, Hongling Pan, Hiuling Chan, Jessica M. Pfliger, Jill A. Rosenfeld, Vanesa C. Lerma, Alyssa Tran, Megan A. Longley, Richard A. Lewis, Monika Weisz-Hubshman, Mir Reza Bekheirnia, Nasim Bekheirnia, Lauren Massingham, Mich Tags: Correction Source Type: research