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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 6
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Short Communications

Hb Sallanches [α104(G11)Cys→Tyr, TGC>TAC] Occurs Frequently on the Indian Subcontinent

Papai Roy Department of Biophysics, Molecular Biology & Bioinformatics, University of Calcutta, Kolkata, India
,
Gargi Bhattacharya Department of Biophysics, Molecular Biology & Bioinformatics, University of Calcutta, Kolkata, India
,
Debasish Banerjee Park Clinic, Kolkata, India
,
Sarmila Chandra Park Clinic, Kolkata, India
,
Malay Ghosh Nil Ratan Sarkar Medical College and Hospital, Kolkata, India
,
Utpal Choudhuri Calcutta Medical College and Hospital, Kolkata, India
,
Manikanchan Das Park Clinic, Kolkata, India
&
Uma B. Dasgupta Department of Biophysics, Molecular Biology & Bioinformatics, University of Calcutta, Kolkata, IndiaCorrespondence[email protected]
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Pages 486-491 | Received 03 Mar 2009, Accepted 16 May 2009, Published online: 03 Dec 2009

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Nikita Mehta, J. Martin Johnston, Molly Hein, Benjamin R. Kipp, Lea Coon, Michelle E. Savedra, James D. Hoyer, Rong He, Aruna Rangan, Min Shi & Jennifer L. Oliveira. (2020) Further Characterization of Hb Bronovo [α103(G10)His→Leu; HBA2: c.311A>T] and First Report of the Homozygous State. Hemoglobin 44:3, pages 174-178.
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Prashant Warang, Sona Nair, Anita Nadkarni, Kanjaksha Ghosh & Roshan B. Colah. (2010) Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches. Hemoglobin 34:1, pages 45-48.
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Articles from other publishers (2)

Pallavi Thaker, Namrata Mahajan, Malay B. Mukherjee & Roshan B. Colah. (2022) Molecular Heterogeneity of Hb H Disease in India. Thalassemia Reports 12:3, pages 73-84.
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Prashant Sharma, Reena Das, Alka Rani Khadwal, Indrani Karmakar, Jasbir Kaur Hira & Sanjeev Chhabra. (2020) HbH disease due to compound heterozygosity for hemoglobins Zürich‐Albisrieden and Sallanches. Pediatric Blood & Cancer 67:4.
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