Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia.

BMC neurology

Volumn 12, Issue , 2012, Pages

  Hedera, Peter ^a   Xiao, Jianfeng ^b   Puschmann, Andreas ^b   Momčilović, Dragana ^b   Wu, Steve W ^b   LeDoux, Mark S ^b  

^a VANDERBILT UNIVERSITY   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; NERVE PROTEIN; PRRT2 PROTEIN, HUMAN;

ADULT; AFRICAN AMERICAN; ARTICLE; CHOREA; ETHNOLOGY; FEMALE; GENETIC PREDISPOSITION; GENETICS; HUMAN; MALE; MIDDLE AGED; MUTATION; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; AFRICAN AMERICANS; CHOREA; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; YOUNG ADULT;

MLCS; MLOWN;

EID: 84866279746     PISSN: None     EISSN: 14712377     Source Type: Journal    
DOI: 10.1186/1471-2377-12-93     Document Type: Article

References (0)