SMPD1 mutations and Parkinson disease.

Dagan, E; Adir, V; Schlesinger, I; Borochowitz, Z; Ayoub, M; Mory, A; Nassar, M; Kurolap, A; Aharon-Peretz, J; Gershoni-Baruch, R

Dagan, E; Adir, V; Schlesinger, I; Borochowitz, Z; Ayoub, M; Mory, A; Nassar, M; Kurolap, A; Aharon-Peretz, J; Gershoni-Baruch, R.

Afiliação

Dagan E; Department of Nursing, Faculty of Social Welfare and Health Sciences, University of Haifa, Haifa, Israel.
Adir V; The Simon Winter Institute for Human Genetics, Bnei Zion Medical Center, Haifa, Israel; The Ruth and Bruce Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
Schlesinger I; The Ruth and Bruce Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel; Department of Neurology and the Cognitive Neurology Institute, Rambam Health Care Campus, Haifa, Israel.
Borochowitz Z; The Simon Winter Institute for Human Genetics, Bnei Zion Medical Center, Haifa, Israel; The Ruth and Bruce Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
Ayoub M; Institute of Human Genetics, Rambam Health Care Campus, Haifa, Israel.
Mory A; Institute of Human Genetics, Rambam Health Care Campus, Haifa, Israel.
Nassar M; Department of Neurology and the Cognitive Neurology Institute, Rambam Health Care Campus, Haifa, Israel.
Kurolap A; Department of Neurology and the Cognitive Neurology Institute, Rambam Health Care Campus, Haifa, Israel.
Aharon-Peretz J; The Ruth and Bruce Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel; Department of Neurology and the Cognitive Neurology Institute, Rambam Health Care Campus, Haifa, Israel.
Gershoni-Baruch R; The Simon Winter Institute for Human Genetics, Bnei Zion Medical Center, Haifa, Israel; Institute of Human Genetics, Rambam Health Care Campus, Haifa, Israel. Electronic address: rgershoni@rambam.health.gov.il.

Parkinsonism Relat Disord ; 21(10): 1296-7, 2015 Oct.

Article em En | MEDLINE | ID: mdl-26318962

Assuntos

Predisposição Genética para Doença/genética; Mutação/genética; Doença de Parkinson/genética; Esfingomielina Fosfodiesterase/genética; Feminino; Humanos; Masculino

Palavras-chave

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

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Esfingomielina Fosfodiesterase / Predisposição Genética para Doença / Mutação Limite: Female / Humans / Male Idioma: En Revista: Parkinsonism Relat Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Israel

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