VIICTR
Profiles
ORIT
Pediatrics CRA
Home
About
Overview
Sharing Data
ORCID
Help
History (2)
A novel pathogenic mutation of MeCP2 impairs chromatin association independent of protein levels.
The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability.
See All 2 Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability.
The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability. Am J Hum Genet. 2022 10 06; 109(10):1923-1931.
View in:
PubMed
subject areas
Animals
DNA, Complementary
Drosophila
Humans
Intellectual Disability
Membrane Proteins
Microcephaly
Microfilament Proteins
Mutation, Missense
Nervous System Malformations
Phenotype
authors with profiles
OGUZ KANCA
HUGO BELLEN
Shenzhao Lu