Identification of rare and novel deletions that cause (δβ)0‐thalassaemia and hereditary persistence of foetal haemoglobin in Indian population期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Identification of rare and novel deletions that cause (δβ)0‐thalassaemia and hereditary persistence of foetal haemoglobin in Indian population

Authors:	Reena Das Neeraj Arora Eunice S. Edison Mammen Chandy Alok Srivastava Shaji R. Velayudhan

Affiliation:	1. Postgraduate Institute of Medical Education and Research, , Chandigarh, India;2. Department of Haematology, Christian Medical College, , Vellore, India;3. Tata Medical Centre, , Kolkata, India;4. Centre for Stem Cell Research, Christian Medical College, , Vellore, India

Abstract:

Keywords:	(δ β )0‐thalassaemia hereditary persistence of foetal haemoglobin haemoglobin β ‐thalassaemia mutation