Ontology highlight
ABSTRACT:
SUBMITTER: Yrigollen CM
PROVIDER: S-EPMC4298645 | biostudies-literature | 2014 Nov
REPOSITORIES: biostudies-literature
Yrigollen Carolyn M CM Sweha Stefan S Durbin-Johnson Blythe B Zhou Lili L Berry-Kravis Elizabeth E Fernandez-Carvajal Isabel I Faradz Sultana Mh SM Amiri Khaled K Shaheen Huda H Polli Roberta R Murillo-Bonilla Luis L Silva Arevalo Gabriel de Jesus Gde J Cogram Patricia P Murgia Alessandra A Tassone Flora F
Intractable & rare diseases research 20141101 4
The CGG trinucleotide repeat within the FMR1 gene is associated with multiple clinical disorders, including fragile X-associated tremor/ataxia syndrome, fragile X-associated primary ovarian insufficiency, and fragile X syndrome. Differences in the distribution and prevalence of CGG repeat length and of AGG interruption patterns have been reported among different populations and ethnicities. In this study we characterized the AGG interruption patterns within 3,065 normal CGG repeat alleles from n ...[more]