Work

A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

Year: 2009

Type: article

Study design: Case Report

Source: Neurogenetics

DOI: 10.1007/s10048-009-0173-5

Authors: C. Pirkevi, S. Lesage, C. Condroyer, H. Tomiyama, N. Hattori, S. Ertan, A. Brice, A. N. Başak

Institutions: Boğaziçi University, Inserm, Université Pierre-et-Marie-Curie, Juntendo University, Istanbul University-Cerrahpaşa, Istanbul University, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital

Language: English

Topic: Parkinson's Disease Mechanisms and Treatments

Subfield: Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Agence Nationale de la Recherche, Boğaziçi Üniversitesi

Award: Pathologie moléculaire et modèles murins du gène LRRK2, impliqué dans la maladie de Parkinson

OpenAlex ID: W2003429238

FWCI: 2.553

Cites: 8

Cited by: 23

Related to: 10