LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact.

Christian Beetz Ana WestenbergerRuslan Al-AliNajim AmezianeNadia AlhashmiRose-Mary BoustanyFuad Al MutairiMajid AlfadhelZuhair Al-HassnanMoenaldeen AlSayedKrishna K KandaswamyOmid PakniaVolha SkrahinaArndt RolfsPeter Bauer

Published in: Movement disorders : official journal of the Movement Disorder Society (2021)

Keyphrases

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genome wide