Identification of rare and novel deletions that cause (...

European Journal of Haematology 2014 / 06 Vol. 92; Iss. 6

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

Mayuranathan, Thiyagaraj, Rayabaram, Janakiram, Das, Reena, Arora, Neeraj, Edison, Eunice S., Chandy, Mammen, Srivastava, Alok, Velayudhan, Shaji R.
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Volume:
92
Language:
english
Journal:
European Journal of Haematology
DOI:
10.1111/ejh.12276
Date:
June, 2014
File:
PDF, 540 KB
english, 2014
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