Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches

Prashant Warang National Institute of Immunohaematology, Indian Council of Medical Research (ICMR), King Edward Memorial Hospital Campus, Mumbai, India

Sona Nair National Institute of Immunohaematology, Indian Council of Medical Research (ICMR), King Edward Memorial Hospital Campus, Mumbai, India

Anita Nadkarni National Institute of Immunohaematology, Indian Council of Medical Research (ICMR), King Edward Memorial Hospital Campus, Mumbai, India

Kanjaksha Ghosh National Institute of Immunohaematology, Indian Council of Medical Research (ICMR), King Edward Memorial Hospital Campus, Mumbai, India

Roshan B. Colah National Institute of Immunohaematology, Indian Council of Medical Research (ICMR), King Edward Memorial Hospital Campus, Mumbai, IndiaCorrespondence[email protected]

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Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches

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Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches

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