Advanced search
Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 46, 2022 - Issue 2
Submit an article Journal homepage
65
Views
1
CrossRef citations to date
0
Altmetric
Brief Communications

Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (HBB: c.255_264delinsTTTTTCTCAG)

Shao-Min Wua Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, People’s Republic of ChinaView further author information
,
Fan Jiangb Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou, People’s Republic of ChinaView further author information
,
Chan Lia Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, People’s Republic of ChinaView further author information
,
Zhen-Tian Guoc Clinical Laboratory, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, People’s Republic of ChinaView further author information
,
Su-Ran Huangd Department of Obstetrics and Gynecology, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, People’s Republic of ChinaView further author information
&
Dong-Zhi Lib Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou, People’s Republic of ChinaCorrespondence[email protected]
View further author information
Pages 129-131 | Received 08 Feb 2022, Accepted 06 May 2022, Published online: 11 Aug 2022

References

  • Wajcman H, Préhu C, Bardakdjian-Michau J, et al. Abnormal hemoglobins: laboratory methods. Hemoglobin. 2001;25(2):169–181.
  • Thom CS, Dickson CF, Gell DA, et al. Hemoglobin variants: biochemical properties and clinical correlates. Cold Spring Harb Perspect Med. 2013;3(3):a011858.
  • Shaji RV, Edison ES, Krishnamoorthy R, et al. Hb Lepore in the Indian population. Hemoglobin. 2003;27(1):7–14.
  • Nieto JM, González FA, Alonso JM, et al. Hb Palencia: a novel δβδ-type two-way fusion variant with β-globin-like expression levels. J Clin Pathol. 2019;72(1):46–51.
  • Shin S-Y, Bang S-M, Kim H-J. A novel hemoglobin variant associated with congenital erythrocytosis: Hb Seoul [β86(F2)Ala→Thr] (HBB:c.259G>A). Ann Clin Lab Sci. 2016;46(3):312–314.
  • Pagano L, Salzano AM, Carbone V, et al. Hb Cardarelli [β86(F2)Ala→Pro]: a new unstable and hyperaffine variant in association with β+-thalassemia. Hemoglobin. 2004;28(2):103–115.
  • Hoyer JD, Wendt PC, Hogan WJ, et al. Hb Nebraska [β86(F2)Ala→Ile (HBB:c.259G>A;260C>T)]: a unique high oxygen affinity hemoglobin variant with a double nucleotide substitution within the same codon. Hemoglobin. 2011;35(1):22–27.
  • Tagawa Y, Fujinami S, Kadota Y, et al. Hb Olomouc [α 2 β 2(86)(F2)Ala→Asp] found in a Japanese family. Hemoglobin. 1992;16(1–2):73–76.
  • Çelebiler A, Aksoy D, Ocakcı S, et al. A new hemoglobin variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T]. Hemoglobin. 2012;36(5):474–479.
  • Qualtieri A, Andreoli V, Crescibene L, et al. Hb Valletta [β 87(F3)Thr→Pro] due to an A→C substitution at codon 87 in a Calabrian family with α-thalassemia. Hemoglobin. 1997;21(1):97–103.
  • Witkowska HE, Lubin BH, Beuzard Y, et al. Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori. N Engl J Med. 1991;325(16):1150–1154.
  • Castro O, Winter WP, Bullock WH, et al. Hemoglobin D Ibadan trait in combination with sigma β thalassemia. Hemoglobin. 1979;3(1):77–82.
  • Zhang H, Li C, Li J, et al. Next-generation sequencing improves molecular epidemiological characterization of thalassemia in Chenzhou Region, P.R. China. J Clin Lab Anal. 2019;33(4):e22845.
  • Achour A, Koopmann TT, Baas F, et al. The evolving role of next-generation sequencing in screening and diagnosis of hemoglobinopathies. Front Physiol. 2021;12:686689.
  • He J, Song W, Yang J, et al. Next-generation sequencing improves thalassemia carrier screening among premarital adults in a high prevalence population: the Dai nationality, China. Genet Med. 2017;19(9):1022–1031.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.