The rs13388259 Intergenic Polymorphism in the Genomic Context of the <i>BCYRN1</i> Gene Is Associated with Parkinson's Disease in the Hungarian Population.

Márki, Sándor; Göblös, Anikó; Szlávicz, Eszter; Török, Nóra; Balicza, Péter; Bereznai, Benjamin; Takáts, Annamária; Engelhardt, József; Klivényi, Péter; Vécsei, László; Molnár, Mária Judit; Nagy, Nikoletta; Széll, Márta

The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson's Disease in the Hungarian Population.

Márki, Sándor; Göblös, Anikó; Szlávicz, Eszter; Török, Nóra; Balicza, Péter; Bereznai, Benjamin; Takáts, Annamária; Engelhardt, József; Klivényi, Péter; Vécsei, László; Molnár, Mária Judit; Nagy, Nikoletta; Széll, Márta.

Afiliación

Márki S; Department of Medical Genetics, University of Szeged, Somogyi u. 4, 6720 Szeged, Hungary.
Göblös A; Department of Dermatology and Allergology, University of Szeged, Korányi fasor 6, 6720 Szeged, Hungary.
Szlávicz E; MTA-SZTE Dermatological Research Group, University of Szeged, Korányi fasor 6, 6720 Szeged, Hungary.
Török N; Department of Dermatology and Allergology, University of Szeged, Korányi fasor 6, 6720 Szeged, Hungary.
Balicza P; Department of Neurology, University of Szeged, Semmelweis u. 6, 6725 Szeged, Hungary.
Bereznai B; Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Tömo u. 25-29, 1083 Budapest, Hungary.
Takáts A; Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Tömo u. 25-29, 1083 Budapest, Hungary.
Engelhardt J; Department of Neurology, Semmelweis University, VIII. Balassa J. u. 6, 1083 Budapest, Hungary.
Klivényi P; Department of Neurology, University of Szeged, Semmelweis u. 6, 6725 Szeged, Hungary.
Vécsei L; Department of Neurology, University of Szeged, Semmelweis u. 6, 6725 Szeged, Hungary.
Molnár MJ; Department of Neurology, University of Szeged, Semmelweis u. 6, 6725 Szeged, Hungary.
Nagy N; MTA-SZTE Neuroscience Research Group, University of Szeged, Semmelweis u. 6, 6725 Szeged, Hungary.
Széll M; Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Tömo u. 25-29, 1083 Budapest, Hungary.

Parkinsons Dis ; 2018: 9351598, 2018.

Article en En | MEDLINE | ID: mdl-29850016

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Parkinsons Dis Año: 2018 Tipo del documento: Article País de afiliación: Hungria Pais de publicación: Estados Unidos

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