Further delineation of the clinical spectrum of de novo TRIM8 truncating mutations.
Am J Med Genet A
; 176(11): 2470-2478, 2018 11.
Article
in En
| MEDLINE
| ID: mdl-30244534
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Carrier Proteins
/
Mutation
/
Nerve Tissue Proteins
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
/
Newborn
Language:
En
Journal:
Am J Med Genet A
Journal subject:
GENETICA MEDICA
Year:
2018
Document type:
Article
Affiliation country:
France
Country of publication:
United States