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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 6
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HB Hillingdon [α46(CE4)Phe→Val (α1 Or α2)]: A New α Chain Hemoglobin Variant

Anna Babb Department of Haematology, Imperial College Healthcare National Health Service (NHS) Trust, Hammersmith Hospital, London, Middlesex, UKCorrespondence[email protected]
,
Susannah Solaiman Spearpoint Surgery, London, Middlesex, UK
,
Brian N. Green Waters MS Technologies Centre, Micromass UK Ltd., Altrincham, Cheshire, UK
,
Debbie Mantio Electrophoresis and Neonatal Screening Department, Central Middlesex Hospital, London, Middlesex, UK
&
Ketan Patel Hillingdon Hospital, London, Middlesex, UK
Pages 503-506 | Received 06 Jun 2009, Accepted 23 Jun 2009, Published online: 03 Dec 2009

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Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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Erin M. Guest, Kathleen A. Neville, James D. Hoyer, Martin K. Safo, Uttam Garg, Carol J. Saunders, Osheiza Abdulmalik & David L. Zwick. (2011) Hb Lake Tapawingo [α46(CE4)Phe→Ser; HBA2:c.140T>C]: A New Unstable α Chain Hemoglobin Variant Associated with Low Systemic Arterial Saturation. Hemoglobin 35:4, pages 411-416.
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