Molecular Characterization of FMR1 Gene by TP-PCR in Women of Reproductive Age and Women with Premature Ovarian Insufficiency

Author:

Dean Deepika Delsa,Agarwal Sarita,Kapoor Deepa,Singh Kuldeep,Vati Chandra

Funder

Council of Science and Industrial Research (CSIR) – New Delhi

intramural project grant , Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Lucknow

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,Genetics,Molecular Medicine,General Medicine

Reference44 articles.

1. Crawford DC, Acuna JM, Sherman SL. FMR1 and the fragile X syndrome: human genome epidemiology review. Genet Med. 2001;3:359–71.

2. Ruiz LR, Borgarello MQ, Aytes LB, Escoda CG. Frile X-syndrome: literature review and report of two cases. Med Oral. 2009;14:9.

3. de Vries BBA, Wiegers AM, Smits APT, Mohkamsing S, Duivenvoorden HJ, Fryns JP, et al. Mental status of females with an FMR1 gene full mutation. Am J Hum Genet. 1996;58:1025–32.

4. Warren ST, Sherman SL. The fragile X syndrome. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular basis of inherited disease, vol. 8. New York: McGraw Hill; 2001. p. 1257–89.

5. Galloway JN, Nelson DL. Evidence for RNA-mediated toxicity in the fragile X-associated tremor/ataxia syndrome. Future Neurol. 2009;4(6):785.

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