Lynne Krohn

Lynne Krohn

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Lynne Krohn

Lynne Krohn

Publications by authors named "Lynne Krohn"

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SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegia.

J Hum Genet 2019 Nov 12;64(11):1145-1151. Epub 2019 Sep 12.

Department of Human Genetics, McGill University, Montréal, QC, Canada.

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http://dx.doi.org/10.1038/s10038-019-0669-2DOI Listing
November 2019

Common and rare GCH1 variants are associated with Parkinson's disease.

Neurobiol Aging 2019 01 15;73:231.e1-231.e6. Epub 2018 Sep 15.

Department of Human Genetics, McGill University, Montréal, Quebec, Canada; Montreal Neurological Institute, McGill University, Montréal, Quebec, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, Quebec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2018.09.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251729PMC
January 2019