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

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

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Veröffentlicht in:Movement disorders 2021-04, Vol.36 (4), p.1029-1031
Hauptverfasser: Beetz, Christian, Westenberger, Ana, Al‐Ali, Ruslan, Ameziane, Najim, Alhashmi, Nadia, Boustany, Rose‐Mary, Al Mutairi, Fuad, Alfadhel, Majid, Al‐Hassnan, Zuhair, AlSayed, Moenaldeen, Kandaswamy, Krishna K., Paknia, Omid, Skrahina, Volha, Rolfs, Arndt, Bauer, Peter
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Sprache:eng
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Humans
Letters: New Observations
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics
LRRK2 protein
Movement disorders
Protein Serine-Threonine Kinases
Rare Diseases
Regular Issue
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container_issue 4
container_start_page 1029
container_title Movement disorders
container_volume 36
creator Beetz, Christian
Westenberger, Ana
Al‐Ali, Ruslan
Ameziane, Najim
Alhashmi, Nadia
Boustany, Rose‐Mary
Al Mutairi, Fuad
Alfadhel, Majid
Al‐Hassnan, Zuhair
AlSayed, Moenaldeen
Kandaswamy, Krishna K.
Paknia, Omid
Skrahina, Volha
Rolfs, Arndt
Bauer, Peter
description
doi_str_mv 10.1002/mds.28452
format Article
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Humans
Letters: New Observations
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics
LRRK2 protein
Movement disorders
Protein Serine-Threonine Kinases
Rare Diseases
Regular Issue
title LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact
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