ARHGEF28 p.Lys280Metfs40Ter in an amyotrophic lateral sclerosis family with a C9orf72 expansion-Reference-Cited by-同舟云学术

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ARHGEF28 p.Lys280Metfs40Ter in an amyotrophic lateral sclerosis family with a C9orf72 expansion

Published:2017-09-22 Issue:5 Volume:3 Page:e190
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Farhan Sali M.K.,Gendron Tania F.,Petrucelli Leonard,Hegele Robert A.,Strong Michael J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),Clinical Neurology

Reference7 articles.

1. Detection of a novel frameshift mutation and regions with homozygosis within ARHGEF28 gene in familial amyotrophic lateral sclerosis

2. ARHGEF28 gene exon 6/intron 6 junction mutations in Chinese amyotrophic lateral sclerosis cohort

3. Genetic and epigenetic study of ALS-discordant identical twins with double mutations inSOD1andARHGEF28

4. El escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis

5. Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

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