Detection of beta-globin gene mutations among Kelantan Malay thalassaemia patients by polymerase chain reaction restriction fragment length polymorphism

Beta-thalassaemia major is an autosomal recessive disorder that results in severe microcytic, hypochromic, haemolytic anaemia among affected patients. Beta-thalassaemia has emerged as one of the most common public health problems in Malaysia, particularly among Malaysian Chinese and Malays. This stu...

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Veröffentlicht in:	Singapore medical journal 2008-12, Vol.49 (12), p.1046-1049
Hauptverfasser:	Rozitah, R, Nizam, M Z, Nur Shafawati, A R, Nor Atifah, M A, Dewi, M, Kannan, T P, Ariffin, N, Norsarwany, M, Setianingsih, I, Harahap, A, Zilfalil, B A
Format:	Artikel
Sprache:	eng
Schlagworte:	beta-Globins - genetics beta-Thalassemia - ethnology beta-Thalassemia - genetics Child Ethnic Groups Humans Malaysia - ethnology Mutation Reverse Transcriptase Polymerase Chain Reaction
Online-Zugang:	Volltext
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