Paper Details

Paper Title

PARK7-Related Early Onset Parkinson Disease in the Setting of Complete Uniparental Isodisomy of Chromosome 1.

Paper Journal Title

Neurol Genet

Paper Citation Count

Paper Publication Year

2021

Bio Mention

Complete Uniparental Isodisomy of Chromosome 1, PARK7, Parkinson Disease

Mesh Descriptor

Author Name	Affiliation
Thomas C Markello	National Human Genome Research Institute (C.X.), MD Office of the Clinical Director (T.M.), National Human Genome Research Institute, MD National Eye Institute (W.M.Z., MD NIH Undiagnosed Diseases Program (C.G.
Catherine Groden	National Human Genome Research Institute (C.X.), MD Office of the Clinical Director (T.M.), National Human Genome Research Institute, MD National Eye Institute (W.M.Z., MD NIH Undiagnosed Diseases Program (C.G.
William A Gahl	National Human Genome Research Institute (C.X.), MD Office of the Clinical Director (T.M.), National Human Genome Research Institute, MD National Eye Institute (W.M.Z., MD NIH Undiagnosed Diseases Program (C.G.
William A Gahl	National Human Genome Research Institute (C.X.), MD Office of the Clinical Director (T.M.), National Human Genome Research Institute, MD National Eye Institute (W.M.Z., MD NIH Undiagnosed Diseases Program (C.G.
Camilo Toro	National Human Genome Research Institute (C.X.), MD Office of the Clinical Director (T.M.), National Human Genome Research Institute, MD National Eye Institute (W.M.Z., MD NIH Undiagnosed Diseases Program (C.G.

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