A nonsense mutation in CHCHD2 in a patient with Parkinson disease.

Authors :: Koschmidder E
Weissbach A
Brüggemann N
Kasten M
Klein C
Lohmann K
Source :: Neurology [Neurology] 2016 Feb 09; Vol. 86 (6), pp. 577-9. Date of Electronic Publication: 2016 Jan 13.
Publication Year :: 2016

Subjects :: Adolescent
Adult
Aged
Child
DNA-Binding Proteins
Female
Genetic Testing methods
Heterozygote
Humans
Male
Middle Aged
Parkinson Disease diagnosis
Young Adult
Codon, Nonsense genetics
Genetic Predisposition to Disease genetics
Mitochondrial Proteins genetics
Parkinson Disease genetics
Transcription Factors genetics

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