Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease
Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease
Where did the research take place?
The study site has not been established. Author addresses may differ from where the research occurred.
Paris, FR · Author affiliation
From the INSERM U289, Neurologie et thérapeutique expérimentale (Drs. Lohmann, Agid, Dürr, and Brice, P. Ibáñez), Département de Génétique, Cytogénétique et Embryologie (Drs. Dürr and Brice), and Fédération de Neurologie, CHU Pitié-Salpêtrière (Drs. Lohmann, Agid, Dürr, and Brice), Hôpital de la Salpêtrière, Paris, France; Department of Clinical and Biological Neurosciences (Dr. Pollak), Service de Neurologie, CHU de Grenoble, France; Federation de Neurologie (Dr. Durif), Service...Location evidence
Grenoble, FR · Author affiliation
From the INSERM U289, Neurologie et thérapeutique expérimentale (Drs. Lohmann, Agid, Dürr, and Brice, P. Ibáñez), Département de Génétique, Cytogénétique et Embryologie (Drs. Dürr and Brice), and Fédération de Neurologie, CHU Pitié-Salpêtrière (Drs. Lohmann, Agid, Dürr, and Brice), Hôpital de la Salpêtrière, Paris, France; Department of Clinical and Biological Neurosciences (Dr. Pollak), Service de Neurologie, CHU de Grenoble, France; Federation de Neurologie (Dr. Durif), Service...Location evidence
A plain-language reading has not been prepared for this paper yet.