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Heterozygous exon 3 deletion in the Parkin gene in a patient with clinical and radiological MSA-C phenotype

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Bibliographic Details
Published in:	Clinical neurology and neurosurgery 2011-06, Vol.113 (5), p.404-406
Main Authors:	Barsottini, Orlando Graziani Povoas, Felício, André Carvalho, de Carvalho Aguiar, Patrícia, Godeiro-Junior, Clécio, Pedroso, Jose Luiz, de Aquino, Camila Catherine Henriques, Bor-Seng-Shu, Edson, de Andrade, Luiz Augusto Franco
Format:	Article
Language:	English
Subjects:	Adult Biological and medical sciences Exons - genetics Female Gene Deletion Heterozygote Humans Hypokinesia - etiology Magnetic Resonance Imaging Medical sciences Mesencephalon - diagnostic imaging Multiple system atrophy Multiple System Atrophy - genetics Multiple System Atrophy - psychology Muscle Rigidity - etiology Mutation - genetics Neurology Neuropsychological Tests Neurosurgery Parkin exon 3 deletion Parkin mutation Phenotype Pons - pathology Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Transcranial sonography Ubiquitin-Protein Ligases - genetics Ultrasonography, Doppler, Transcranial
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