First Observation of Hb Lepore Hollandia in the Baiga Tribal Family

Author:

Lad Harsha,Yadav Manju,Mehta Pallavi,Patel Purushottam,Sawant Pratibha,Colah Roshan B.,Mukherjee Malay B.,Shanmugam RajasubramaniamORCID

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Reference12 articles.

1. Bozkurt G, Baysal E, Gu L-H, Huisman THJ (1994) Thalassemia intermedia in two patients with Hb Lepore-β0-thalassemia (Frameshift codon 8,-AA). Hemoglobin 18(3):247–250

2. Chakova L, Spasova M, Genev E (1998) Thalassemia intermedia in an infant. Folia Med 40(1):84–87

3. Sreedharanunni S, Chhabra S, Kaur JH, Bansal D, Sharma P, Das R (2015) β-thalassemia intermedia caused by compound heterozygosity for Hb Lepore-Hollandia and β-thalassemia is rare in the Indian Population. Hemoglobin 39(5):362–365

4. Labie D, Schroeder WA, Huisman THJ (1966) The amino acid sequence of the δ-β chains of Hemoglobin Lepore-Augusta = Lepore Washington. Biochim Biophys Acta 127(2):428–437

5. Ostertag W, Smith EW (1969) Hemoglobin-Lepore-Baltimore, a third type of a δβ crossover (δ50, β86). Eur J Biochem 10(2):371–376

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