The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability
Am J Hum Genet
.
2022 Nov 3;109(11):2092.
doi: 10.1016/j.ajhg.2022.10.001.
Authors
Yan Huang
,
Gabrielle Lemire
,
Lauren C Briere
,
Fang Liu
,
Marja W Wessels
,
Xueqi Wang
,
Matthew Osmond
,
Oguz Kanca
,
Shenzhao Lu
,
Frances A High
,
Melissa A Walker
,
Lance H Rodan
;
Undiagnosed Diseases Network
;
Care4Rare Canada Consortium
;
Michael F Wangler
,
Shinya Yamamoto
,
Kristin D Kernohan
,
David A Sweetser
,
Kym M Boycott
,
Hugo J Bellen
PMID:
36332614
PMCID:
PMC9674957
DOI:
10.1016/j.ajhg.2022.10.001
No abstract available
Publication types
Published Erratum