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

Authors :
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
Source :
Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2021 Apr; Vol. 36 (4), pp. 1029-1031. Date of Electronic Publication: 2021 Jan 12.
Publication Year :
2021

Subjects

Subjects :
Humans
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 genetics
Protein Serine-Threonine Kinases
Rare Diseases

Details

Language :
English
ISSN :
1531-8257
Volume :
36
Issue :
4
Database :
MEDLINE
Journal :
Movement disorders : official journal of the Movement Disorder Society
Publication Type :
Editorial & Opinion
Accession number :
33433017
Full Text :
https://doi.org/10.1002/mds.28452
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