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Kufor‐Rakeb Syndrome Due to a Novel ATP 13A2 Mutation in 2 Chinese‐American Brothers
Author(s) -
Noch Evan,
Henchcliffe Claire,
Hellmers Natalie,
Chu Mary Lynn,
Pappas John,
Moran Ellen,
Alcaraz Wendy,
Sarva Harini
Publication year - 2017
Publication title -
movement disorders clinical practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.754
H-Index - 18
ISSN - 2330-1619
DOI - 10.1002/mdc3.12567
Subject(s) - mutation , genetics , psychology , biology , gene
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