Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects-Reference-Cited by-同舟云学术

Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects

Published:2020-07 Issue:1 Volume:107 Page:96-110
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Kim Kyung-Hee,Hong Eun Pyo,Shin Jun Wan,Chao Michael J.,Loupe Jacob,Gillis Tammy,Mysore Jayalakshmi S.,Holmans Peter,Jones Lesley,Orth Michael,Monckton Darren G.,Long Jeffrey D.,Kwak Seung,Lee Ramee,Gusella James F.,MacDonald Marcy E.,Lee Jong-Min

Funder

National Institutes of Health

NIH

National Institute of Neurological Disorders and Stroke

NINDS

Cure Huntington's Disease Initiative (CHDI) Foundation

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes;Cell,1993

2. Huntington disease;Bates;Nat. Rev. Dis. Primers,2015

3. The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease;Keum;Am. J. Hum. Genet.,2016

4. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington’s disease;Andrew;Nat. Genet.,1993

5. Trinucleotide repeat length instability and age of onset in Huntington’s disease;Duyao;Nat. Genet.,1993

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