Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44

Author:

Watson Lauren M.,Bamber Elizabeth,Schnekenberg Ricardo Parolin,Williams Jonathan,Bettencourt Conceição,Lickiss Jennifer,Jayawant Sandeep,Fawcett Katherine,Clokie Samuel,Wallis Yvonne,Clouston Penny,Sims David,Houlden Henry,Becker Esther B.E.,Németh Andrea H.

Funder

the Marie Skłodowska-Curie

John Fell OUP Fund

Action Medical Research

Henry Smith Charity

CNPq (National Council for Scientific and Technological Development), Brazil

Medical Research Council (UK) Computational Genomics Analysis and Training programme

Wellcome Trust in Equipment and Strategic Award (Synaptopathies) funding

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference42 articles.

1. Chemical excitation of spinal neurones;Curtis;Nature,1959

2. Cellular and circuit mechanisms underlying spinocerebellar ataxias;Meera;J. Physiol.,2016

3. Are Type 1 metabotropic glutamate receptors a viable therapeutic target for the treatment of cerebellar ataxia?;Power;J. Physiol.,2016

4. The metabotropic glutamate receptor 1, GRM1: evaluation as a candidate gene for inherited forms of cerebellar ataxia;Rossi;J. Neurol.,2010

5. Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1;Guergueltcheva;Am. J. Hum. Genet.,2012

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