Exome Sequencing Identifies a Novel Homozygous Missense
ATP13A2
Mutation
Mov Disord Clin Pract
.
2016 Apr 26;4(1):132-135.
doi: 10.1002/mdc3.12353.
eCollection 2017 Jan-Feb.
Authors
Masoom M Abbas
1
,
Shyla T Govindappa
1
,
Una-Marie Sheerin
2
,
Kailash P Bhatia
3
,
Uday B Muthane
1
Affiliations
1
Parkinson's and Ageing Research Foundation Bangalore India.
2
Department of Molecular Neuroscience UCL Institute of Neurology University College London London United Kingdom.
3
UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London United Kingdom.
PMID:
30713959
PMCID:
PMC6353396
DOI:
10.1002/mdc3.12353
No abstract available
Keywords:
Kufor‐Rakeb syndrome; early onset atypical parkinsonism; exome sequence.
Publication types
Case Reports