Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria.
Am J Med Genet A
; 155A(9): 2071-7, 2011 Sep.
Article
in En
| MEDLINE
| ID: mdl-21834044
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Abnormalities, Multiple
/
Malformations of Cortical Development
/
Exome
/
Nerve Tissue Proteins
Type of study:
Prognostic_studies
Limits:
Adult
/
Child
/
Female
/
Humans
/
Male
Language:
En
Journal:
Am J Med Genet A
Journal subject:
GENETICA MEDICA
Year:
2011
Document type:
Article
Affiliation country:
United States