Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island

208Citations
Citations of this article
67Readers
Mendeley users who have this article in their library.
Get full text

References Powered by Scopus

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

3152Citations
N/AReaders
Get full text

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1382Citations
N/AReaders
Get full text

Absence of expression of the FMR-1 gene in fragile X syndrome

1315Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α(1A)-voltage-dependent calcium channel

1491Citations
N/AReaders
Get full text

Trinucleotide repeat disorders

1185Citations
N/AReaders
Get full text

A literature network of human genes for high-throughput analysis of gene expression

669Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Gu, Y., Shen, Y., Gibbs, R. A., & Nelson, D. L. (1996). Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island. Nature Genetics, 13(1), 109–113. https://doi.org/10.1038/ng0596-109

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 22

52%

Researcher 13

31%

Professor / Associate Prof. 7

17%

Readers' Discipline

Tooltip

Agricultural and Biological Sciences 22

50%

Biochemistry, Genetics and Molecular Bi... 12

27%

Medicine and Dentistry 6

14%

Neuroscience 4

9%

Article Metrics

Tooltip
Mentions
References: 4

Save time finding and organizing research with Mendeley

Sign up for free