MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects.
Hum Genet
; 141(1): 65-80, 2022 Jan.
Article
in En
| MEDLINE
| ID: mdl-34748075
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Transcription Factors
/
Genetic Variation
/
Neurodevelopmental Disorders
/
Nerve Tissue Proteins
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Hum Genet
Year:
2022
Document type:
Article
Affiliation country:
Country of publication: