C9orf72 Hexanucleotide Repeat Expansions as the Causative Mutation for Chromosome 9p21–Linked Amyotrophic Lateral Sclerosis and Frontotemporal Dementia - Concepedia

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C9orf72 Hexanucleotide Repeat Expansions as the Causative Mutation for Chromosome 9p21–Linked Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

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Citations

12

References

2012

Year

Hussein Daoud, Hamid Suhail, Mike Sabbagh, Véronique Belzil, Anna Szuto, Alexandre Dionne‐Laporte, Jawad Khoris, William Camu, François Salachas, Vincent Meininger,

Archives of Neurology

Abstract

Our findings further confirm the C9orf72 hexanucleotide repeat expansion as the causative mutation for c9ALS/FTD and strengthen the hypothesis that ALS and FTD belong to the same disease spectrum.

References

	Year	Citations

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