GNAL mutations and dystonia - In reply

K.R. Kumar; K.A. Martemyanov; K. Lohmann

doi:10.1001/jamaneurol.2014.1509

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Journal article

GNAL mutations and dystonia - In reply

K.R. Kumar, K.A. Martemyanov and K. Lohmann

JAMA Neurology, Vol.71(8), p.1053

2014

DOI: https://doi.org/10.1001/jamaneurol.2014.1509

PMID: 25111209

Abstract

Female

GTP-Binding Protein alpha Subunits

Humans

Male

Mutation

Torticollis

guanine nucleotide binding protein alpha subunit

cervical dystonia

disease activity

dystonia

exon

gene

gene function

gene identification

gene location

gene mutation

genetic screening

GNAL gene

human

letter

molecular pathology

outcome assessment

priority journal

promoter region

segmental dystonia

sequence analysis

female

genetics

male

mutation

torticollis

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Web Of Science research areas: Clinical Neurology
ESI research areas: Neuroscience & Behavior

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Details

Title: GNAL mutations and dystonia - In reply
Creators: K.R. Kumar - University of Lübeck
K.A. Martemyanov - Scripps Research Institute
K. Lohmann - University of Lübeck
Publication Details: JAMA Neurology, Vol.71(8), p.1053
Publisher: American Medical Association
Comment: Export Date: 24 October 2025; Cited By: 1
Academic Unit: Physiology and Biophysics Research; Miller School of Medicine
Resource Type: Journal article
PMID: 25111209
Record Identifier: 991032828750102976