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

Christian Beetz*, Ana Westenberger, Ruslan Al-Ali, Najim Ameziane, Nadia Alhashmi, Rose Mary Boustany, Fuad Al Mutairi, Majid Alfadhel, Zuhair Al-Hassnan, Moenaldeen AlSayed, Krishna K. Kandaswamy, Omid Paknia, Volha Skrahina, Arndt Rolfs, Peter Bauer

*Corresponding author for this work
Original languageEnglish
JournalMovement Disorders
Issue number4
Pages (from-to)1029-1031
Number of pages3
Publication statusPublished - 04.2021

Research Areas and Centers

  • Research Area: Medical Genetics

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