Mutation Analysis of Beta-thalassaemia in 30 Families of India: A Report

Introduction: The β-thalassaemia is one of the haemoglobinopathies related to genetic disorders. It occurs due to mutation in β-gene of autosome 11. In India, it affects 1-7% of couples annually. Reports are available in few states of India about β-thalassaemia affected families. But much data is no...

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Autors principals:	Parth S Shah, Nidhi D Shah, Hari Shankar P Ray, Nikunj B Khatri, Ketan K Vaghasia, Mandava V Rao, Sandip C Shah
Format:	Artigo
Idioma:	Inglês
Publicat:	JCDR Research and Publications Private Limited 2018-05-01
Col·lecció:	Journal of Clinical and Diagnostic Research
Matèries:	beta-thalassaemia traits red cell markers referral cases
Accés en línia:	https://jcdr.net/articles/PDF/11463/27646_F(SHU)_PF1(AJ_BT_AP)_PFA(AJ_SL)_PB(BT_SL)_PN(SL).pdf
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