Epileptic encephalopathy and atypical Rett syndrome with mutations in CDKL5: clinical and molecular characterization of two Brazilian patients / Encefalopatia epilética e síndrome de Rett atípica por mutações no gene CDKL5: caracterização clínica e molecular de dois casos brasileiros
Arq. neuropsiquiatr
;
71(6): 414-415, jun. 2013. graf
Article
in English
| LILACS
| ID: lil-677601
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Spasms, Infantile
/
Rett Syndrome
/
Protein Serine-Threonine Kinases
/
Mutation
Limits:
Female
/
Humans
/
Infant
Country/Region as subject:
South America
/
Brazil
Language:
English
Journal:
Arq. neuropsiquiatr
Journal subject:
Neurology
/
Psychiatry
Year:
2013
Type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
Faculdade Evangélica do Paraná/BR
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