Current research, diagnosis, and treatment of fragile X-associated tremor/ataxia syndrome-Reference-Cited by-同舟云学术

Current research, diagnosis, and treatment of fragile X-associated tremor/ataxia syndrome

Published:2014 Issue:4 Volume:3 Page:101-109
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Muzar Zukhrofi¹,Lozano Reymundo¹

Affiliation:

1. UC Davis MIND Institute and Department of Pediatrics, UC Davis Medical Center

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Reference104 articles.

1. 1. Cronister A, Schreiner R, Wittenberger M, Amiri K, Harris K, Hagerman RJ. Heterozygous fragile X female: Historical, physical, cognitive, and cytogenetic features. Am J Med Genet. 1991; 38:269-274.

2. 2. Mazzocco MM, Pennington BF, Hagerman RJ. The neurocognitive phenotype of female carriers of fragile X: Additional evidence for specificity. J Dev Behav Pediatr. 1993; 14:328-335.

3. 3. Reiss AL, Freund L, Abrams MT, Boehm C, Kazazian H.Neurobehavioral effects of the fragile X premutation in adult women: A controlled study. Am J Hum Genet. 1993; 52:884-894.

4. 4. Rousseau F, Heitz D, Tarleton J, et al. A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: The first 2,253 cases. Am J Med Genet. 1994; 55:225-237.

5. 5. Hagerman R, Hagerman P. Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome. Lancet Neurol. 2013; 12:786-798.

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