Lack of evidence for association of UQCRC1 with autosomal dominant Parkinson's disease in Caucasian families
Neurogenetics
.
2021 Oct;22(4):365-366.
doi: 10.1007/s10048-021-00647-4.
Epub 2021 Jul 21.
Authors
Thomas Courtin
1
2
,
Christelle Tesson
1
,
Jean-Christophe Corvol
1
3
,
Suzanne Lesage
1
,
Alexis Brice
4
5
;
French Parkinson’s disease genetics (PDG) group
Affiliations
1
Sorbonne Université, INSERM, CNRS, Institut du Cerveau - Paris Brain Institute - ICM, 75013, Paris, France.
2
Hôpital Pitié-Salpêtrière, DMU BioGe'M, AP-HP, 75013, Paris, France.
3
Hôpital Pitié-Salpêtrière, DMU Neuroscience, AP-HP, 75013, Paris, France.
4
Sorbonne Université, INSERM, CNRS, Institut du Cerveau - Paris Brain Institute - ICM, 75013, Paris, France. alexis.brice@icm-institute.org.
5
Hôpital Pitié-Salpêtrière, DMU BioGe'M, AP-HP, 75013, Paris, France. alexis.brice@icm-institute.org.
PMID:
34286409
DOI:
10.1007/s10048-021-00647-4
No abstract available
Publication types
Letter
Comment
MeSH terms
Arthrogryposis*
Humans
Mutation
Parkinson Disease* / genetics
White People / genetics