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C9orf72 repeat expansions are not detected in Chinese patients with familial ALS

22 Jul 2013

Abstract excerpt

Recently, a hexanucleotide repeat (GGGGCC) expansion in the chromosome 9 open reading frame 72 gene (C9orf72) was reported as a major cause of amyotrophic lateral sclerosis (ALS) and frontotemporal...

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Amyotrophic Lateral Sclerosis Research
Neurogenetic and Muscular Disorders Research
Neurological diseases and metabolism

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23869403
DOI: 10.3109/21678421.2013.817588

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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