Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay.
Genet Med
; 20(7): 778-784, 2018 07.
Article
in En
| MEDLINE
| ID: mdl-28837161
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Membrane Proteins
/
Intellectual Disability
/
Nerve Tissue Proteins
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Female
/
Humans
/
Male
Country/Region as subject:
Asia
Language:
En
Journal:
Genet Med
Journal subject:
GENETICA MEDICA
Year:
2018
Type:
Article
Affiliation country:
Switzerland