The FMR–1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

Author:

Devys Didier,Lutz Yves,Rouyer Nicolas,Bellocq Jean-Pierre,Mandel Jean-Louis

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference36 articles.

1. Sherman, S. Recognition of the fragile X or Martin-Bell syndrome. In Fragile X syndrome: diagnosis, treatment and research. (eds Hagerman, R.J. & Silverman A.C.) 69–97 (The Johns Hopkins University Press, Baltimore, 1991).

2. Sutherland, G.R. Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium. Science 197, 265–266 (1977).

3. Hagermann et al. Physical and behavioral phenotype. In Fragile Xsyndrome: diagnosis, treatment and research. (eds Hagerman, R.J. & Silverman A.C.) 3–68 (The Johns Hopkins University Press, Baltimore, 1991).

4. Sherman, S.L. et al. Further segragation analysis of the fragile X syndrome with special reference to transmitting males. Hum. Genet. 69, 289–299 (1985).

5. Oberlé, I. et al. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome. Science 252, 1097–1102 (1991).

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