Analisis genetik molekul pesakit Sindrom Fragile X di Hospital Universiti Sains Malaysia (HUSM)

Sindrom Fragile X merupakan salah satu penyakit pewarisan yang paling kerap menyebabkan keadaan kerencatan akal. Penyakit ini berlaku disebabkan oleh peningkatan jujukan trinukleotida ulangan (CGG) yang terletak dalam kawasan 5' UTR gen FMR1 dan mengakibatkan perencatan fungsi gen ini. Sindr...

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Bibliographic Details
Main Author:	Sidek, Mohamad Ros
Format:	Thesis
Language:	English
Published:	2006
Subjects:	R Medicine (General)
Online Access:	http://eprints.usm.my/47736/
Abstract	Abstract here

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