Heterozygous exon 3 deletion in the Parkin gene in a patient with clinical and radiological MSA-C phenotype
| Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
|---|---|
| Data(s) |
19/10/2012
19/10/2012
2011
|
| Resumo |
Fondation Philantropique |
| Identificador |
CLINICAL NEUROLOGY AND NEUROSURGERY, v.113, n.5, p.404-406, 2011 0303-8467 http://producao.usp.br/handle/BDPI/23384 10.1016/j.clineuro.2010.11.015 |
| Idioma(s) |
eng |
| Publicador |
ELSEVIER SCIENCE BV |
| Relação |
Clinical Neurology and Neurosurgery |
| Direitos |
restrictedAccess Copyright ELSEVIER SCIENCE BV |
| Palavras-Chave | #Parkin mutation #Multiple system atrophy #Parkin exon 3 deletion #Transcranial sonography #MULTIPLE SYSTEM ATROPHY #BRAIN PARENCHYMA SONOGRAPHY #CONSENSUS STATEMENT #SUBSTANTIA-NIGRA #DISEASE #MUTATIONS #DIAGNOSIS #FAMILY #ONSET #Clinical Neurology #Surgery |
| Tipo |
article original article publishedVersion |
