SMPD1 mutations and Parkinson disease

Parkinsonism and Related Disorders

Volumn 21, Issue 10, 2015, Pages 1296-1297

  Dagan, E ^a   Adir, V ^b,c   Schlesinger, I ^c,d   Borochowitz, Z ^b,c   Ayoub, M ^e   Mory, A ^e   Nassar, M ^d   Kurolap, A ^d   Aharon Peretz, J ^c,d   Gershoni Baruch, R ^c,e  

^a UNIVERSITY OF HAIFA   (Israel)

^b BNAI ZION MEDICAL CENTER   (Israel)

^c TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^d Department of Neurology and the Cognitive Neurology Institute ^*  (Israel)

^e Institute of Human Genetics   (Israel)

Author keywords

Gaucher disease; GBA; Niemann Pick disease; Parkinson's disease; SMPD1

Indexed keywords

GBA GENE; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC RISK; HETEROZYGOTE; HUMAN; LETTER; PARKINSON DISEASE; PRIORITY JOURNAL; SMPD1 GENE; FEMALE; GENETICS; MALE; MUTATION;

SPHINGOMYELIN PHOSPHODIESTERASE;

FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MUTATION; PARKINSON DISEASE; SPHINGOMYELIN PHOSPHODIESTERASE;

EID: 84942195361     PISSN: 13538020     EISSN: 18735126     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2015.08.019     Document Type: Letter

References (8)

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