VIICTR
Profiles
ORIT
Pediatrics CRA
Home
About
Overview
Sharing Data
ORCID
Help
History (1)
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
See All 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
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. J Med Genet. 2017 02; 54(2):84-86.
View in:
PubMed
subject areas
Child
Child, Preschool
Exome
Female
High-Throughput Nucleotide Sequencing
Humans
Intellectual Disability
Male
Muscle Hypotonia
Mutation, Missense
Neurodevelopmental Disorders
Tumor Protein p73
Ubiquitin-Protein Ligases
authors with profiles
GEOFFREY PREIDIS