Results 161 to 170 of about 117,772 (258)

Allele-specific silencing of a dominant SETX mutation in familial amyotrophic lateral sclerosis type 4. [PDF]

open access: yesHGG Adv
Winkelsas A   +7 more
europepmc   +1 more source

MIDN locus structural variants and Parkinson's Disease risk

open access: yesAnnals of Clinical and Translational Neurology, 2020
Kimberley J. Billingsley   +6 more
doaj   +1 more source

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