Hair root FMRP expression for screening of fragile X full mutation females

Hair root FMRP expression for screening of fragile X full mutation females

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The fragile X syndrome is the most common form of inherited mental retardation in humans, caused by an expansion of the cytosine-guanine-guanine (CGG) repeat in the fragile X mental retardation 1 (FMR1) gene located on the X chromosome. Antibody tests have been developed to identify fragile X patien...

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Bibliographic Details
Main Authors: Lantip Rujito, Dwi Kustiani, Lies Anne Severijnen, Peter Hanzon, Sultana MH Faradz, Rob Willemsen
Format: Article
Language:English
Published: Faculty of Medicine Trisakti University 2011-04-01
Series:Universa Medicina
Subjects:
Fragile X syndrome
full mutation females
cognitive functioning
Online Access:http://www.univmed.org/wp-content/uploads/2011/04/Lantip1.pdf

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http://www.univmed.org/wp-content/uploads/2011/04/Lantip1.pdf

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