Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb].

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. Fragile X...

書目詳細資料
主要作者:	Sidek, Mohamad Ros
格式:	Thesis
語言:	英语
出版:	2006
主題:	RJ370-550 Diseases of children and adolescents
在線閱讀:	http://eprints.usm.my/8366/

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