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

doi:10.1002/mds.28452

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

Institute of Neurogenetics

9 Citations (Scopus)

Original language	English
Journal	Movement Disorders
Volume	36
Issue number	4
Pages (from-to)	1029-1031
Number of pages	3
ISSN	0885-3185
DOIs	https://doi.org/10.1002/mds.28452
Publication status	Published - 04.2021

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Beetz, C., Westenberger, A., Al-Ali, R., Ameziane, N., Alhashmi, N., Boustany, R. M., Al Mutairi, F., Alfadhel, M., Al-Hassnan, Z., AlSayed, M., Kandaswamy, K. K., Paknia, O., Skrahina, V., Rolfs, A., & Bauer, P. (2021). LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact. Movement Disorders, 36(4), 1029-1031. https://doi.org/10.1002/mds.28452

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

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

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Beetz, C, Westenberger, A, Al-Ali, R, Ameziane, N, Alhashmi, N, Boustany, RM, Al Mutairi, F, Alfadhel, M, Al-Hassnan, Z, AlSayed, M, Kandaswamy, KK, Paknia, O, Skrahina, V, Rolfs, A & Bauer, P 2021, 'LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact', Movement Disorders, vol. 36, no. 4, pp. 1029-1031. https://doi.org/10.1002/mds.28452

TY - JOUR

T1 - LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact

AU - Beetz, Christian

AU - Westenberger, Ana

AU - Al-Ali, Ruslan

AU - Ameziane, Najim

AU - Alhashmi, Nadia

AU - Boustany, Rose Mary

AU - Al Mutairi, Fuad

AU - Alfadhel, Majid

AU - Al-Hassnan, Zuhair

AU - AlSayed, Moenaldeen

AU - Kandaswamy, Krishna K.

AU - Paknia, Omid

AU - Skrahina, Volha

AU - Rolfs, Arndt

AU - Bauer, Peter

PY - 2021/4

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UR - https://www.mendeley.com/catalogue/6ea90a9d-6048-3072-937e-43d497e367f3/

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DO - 10.1002/mds.28452

M3 - Journal articles

C2 - 33433017

AN - SCOPUS:85099174511

SN - 0885-3185

VL - 36

SP - 1029

EP - 1031

JO - Movement Disorders

JF - Movement Disorders

IS - 4

ER -

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

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