Kufor-Rakeb Syndrome Due to a Novel ATP13A2 Mutation in 2 Chinese-American Brothers
Mov Disord Clin Pract
.
2017 Dec 21;5(1):92-95.
doi: 10.1002/mdc3.12567.
eCollection 2018 Jan-Feb.
Authors
Evan Noch
1
,
Claire Henchcliffe
1
,
Natalie Hellmers
1
,
Mary Lynn Chu
2
,
John Pappas
3
,
Ellen Moran
4
,
Wendy Alcaraz
5
,
Harini Sarva
1
Affiliations
1
Department of Neurology Weill Cornell Medicine New York-Presbyterian Hospital New York New York USA.
2
Department of Neurology New York University Langone Medical Center New York New York USA.
3
Department of Pediatrics New York University Langone Medical Center New York New York USA.
4
Center for Children New York University Hospital for Joint Diseases New York New York USA.
5
Ambry Genetics Aliso Viejo California USA.
PMID:
30746398
PMCID:
PMC6336435
DOI:
10.1002/mdc3.12567
No abstract available
Keywords:
Kufor‐Rakeb Syndrome; Parkinson's disease; movement disorders.
Publication types
Case Reports