Somatic Expansion in Mouse and Human Carriers of Fragile X Premutation Alleles-Reference-Cited by-同舟云学术

Somatic Expansion in Mouse and Human Carriers of Fragile X Premutation Alleles

Published:2012-10-04 Issue:1 Volume:34 Page:157-166
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Lokanga Rachel Adihe¹,Entezam Ali,Kumari Daman¹,Yudkin Dmitry¹,Qin Mei²,Smith Carolyn Beebe²,Usdin Karen¹

Affiliation:

1. Section on Gene Structure and Disease; National Institute of Diabetes; Digestive and Kidney Diseases; National Institutes of Health; Bethesda; Maryland

2. Section on Neuroadaptation and Protein Metabolism; National Institute of Mental Health; National Institutes of Health; Bethesda; Maryland

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference60 articles.

1. Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study-preliminary data;Allingham-Hawkins;Am J Med Genet,1999

2. Examination of factors associated with instability of the FMR1 CGG repeat;Ashley-Koch;Am J Hum Genet,1998

3. Growth and aging in the rat: changes in total protein, cellularity, and polyploidy in various organs;Bohman;J Exp Zool,1985

4. Steady-state regulation of the human DNA mismatch repair system;Chang;J Biol Chem,2000

5. Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1;Chong;Nat Genet,1995

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