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

Journal article

Peer reviewed

Christian Beetz, Ana Westenberger, Ruslan Al-Ali, Najim Ameziane, Nadia Alhashmi, Rose-Mary Boustany, Fuad Al Mutairi, Majid Alfadhel, Zuhair Al-Hassnan, Moenaldeen AlSayed, …

Movement disorders, Vol.36(4), pp.1029-1031

04/2021

PMID: 33433017

Abstract

Clinical Neurology

Life Sciences & Biomedicine

Neurosciences & Neurology

Science & Technology

1 Record Views

Title: LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact
Creators - without role: Christian Beetz - Centogene
Ana Westenberger - Centogene
Ruslan Al-Ali - Centogene
Najim Ameziane - Centogene
Nadia Alhashmi - Royal Hosp, Natl Genet Ctr, Muscat, Oman
Rose-Mary Boustany - American University of Beirut Medical Center
Fuad Al Mutairi - King Abdulaziz Medical City
Majid Alfadhel - King Saud bin Abdulaziz University for Health Sciences
Zuhair Al-Hassnan - King Faisal Specialist Hospital & Research Centre
Moenaldeen AlSayed - Alfaisal University
Krishna K. Kandaswamy - Centogene
Omid Paknia - Centogene
Volha Skrahina - Centogene
Arndt Rolfs - Centogene
Peter Bauer - Centogene
Publication Details: Movement disorders, Vol.36(4), pp.1029-1031
Publisher: Wiley
Number of pages: 3
Identifiers: 9913791308331
Academic Unit: King Faisal University; Alfaisal University; King Abdulaziz University; King Saud Bin Abdulaziz University for Health Sciences
Language: English
Resource Type: Journal article