[Alternating hemiplegia of childhood: ATP1A3 gene analysis in 16 patients]. / Hemiplejía alternante de la infancia: estudio del gen ATP1A3 en 16 pacientes.
Med Clin (Barc)
; 143(1): 25-8, 2014 Jul 07.
Article
in Es
| MEDLINE
| ID: mdl-24768197
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Ocular Motility Disorders
/
Point Mutation
/
Sodium-Potassium-Exchanging ATPase
/
Mutation, Missense
/
Dystonic Disorders
/
Hemiplegia
Type of study:
Observational_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
Country/Region as subject:
Europa
Language:
Es
Journal:
Med Clin (Barc)
Year:
2014
Document type:
Article
Country of publication:
Spain