Expanding the clinical phenotype of DYT5 mutations: is multiple system atrophy a possible one?
Neurology
.
2013 Jul 16;81(3):301-2.
doi: 10.1212/WNL.0b013e31829bfd7c.
Epub 2013 Jun 14.
Authors
Roberto Ceravolo
1
,
Valentina Nicoletti
,
Barbara Garavaglia
,
Chiara Reale
,
Lorenzo Kiferle
,
Ubaldo Bonuccelli
Affiliation
1
University of Pisa, Pisa, Italy. r.ceravolo@med.unipi.it
PMID:
23771491
DOI:
10.1212/WNL.0b013e31829bfd7c
No abstract available
Publication types
Case Reports
MeSH terms
Aged
Female
GTP Cyclohydrolase / genetics*
Humans
Multiple System Atrophy / diagnosis
Multiple System Atrophy / genetics*
Mutation
Neurologic Examination
Phenotype
Substances
GTP Cyclohydrolase