The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome.
Hum Mol Genet
; 25(3): 558-70, 2016 Feb 01.
Article
in En
| MEDLINE
| ID: mdl-26647311
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Rett Syndrome
/
Mutation, Missense
/
Alleles
/
Methyl-CpG-Binding Protein 2
Type of study:
Prognostic_studies
Limits:
Animals
/
Humans
/
Male
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2016
Document type:
Article
Affiliation country:
Reino Unido
Country of publication:
Reino Unido