Advanced search
Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 6
Submit an article Journal homepage
108
Views
3
CrossRef citations to date
0
Altmetric
Short Communications

HB Fannin-Lubbock-I with A Single GGC>GAC Mutation at β119(GH2)Gly→Asp in a Homozygous Mexican Patient

Bertha Ibarra División de Genética, Centro de Investigación Biomédica de Occidente, CMNO, IMSS, Guadalajara, Jalisco, México; Doctorado en Genética Humana, Centro Universitario en Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, MéxicoCorrespondence[email protected]
,
Edna Aizpuru Servicio de Genética Hospital Ángeles del Pedregal, DF México
,
J. Yoaly Sánchez-López División de Genética, Centro de Investigación Biomédica de Occidente, CMNO, IMSS, Guadalajara, Jalisco, México; Doctorado en Genética Humana, Centro Universitario en Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, México
,
Karina R. Morales División de Genética, Centro de Investigación Biomédica de Occidente, CMNO, IMSS, Guadalajara, Jalisco, México; Doctorado en Genética Humana, Centro Universitario en Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, México
,
Francisco J. Perea División de Genética, Centro de Investigación Biomédica de Occidente, CMNO, IMSS, Guadalajara, Jalisco, México; Doctorado en Genética Humana, Centro Universitario en Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, México
&
Guillermo Ruiz-Reyes Laboratorios Clínicos de Puebla, Puebla, México
Pages 492-497 | Received 05 Nov 2008, Accepted 22 Apr 2009, Published online: 03 Dec 2009

REFERENCES

  • Moo-Penn WF, Bechtel KC, Johnson MH, . Hemoglobin Fannin-Lubbock [α2β2119(GH2) Gly→Asp]. A new hemoglobin variant at the α1β1 contact. Biochim Biophys Acta. 1976;453(2):472–477.
  • Schneider RG, Berkman NL, Brimhall B, Jones RT. Hemoglobin Fannin-Lubbock α2β2119(GH2) Gly→Asp]. A slightly unstable mutant. Biochim Biophys Acta. 1976;453(2):478–483.
  • Qin WB, Pobedimskaya DD, Molchanova TP, . Hb Fannin-Lubbock in five Spanish families is characterized by two mutations: β111 GTC→CTC (Val→Leu) and β119 GGC→GAC (Gly→Asp). Hemoglobin. 1994;18(4–5):297–306.
  • González FA, Ropero P, Arrizabalaga B, García P, Cela E, Villegas A. Fannin-Lubbock II hemoglobin [β111 (G13) Val→Leu and β119 (GH2) Gly→Asp]: description of four new cases. Medicina Clínica (Barc). 2007;129(10):379–381.
  • Ibarra B, Vaca G, Franco-Gamboa E, . Abnormal hemoglobins in Northwestern Mexico. Acta Anthropogenet. 1982;6(4):217–223.
  • Huisman THJ, Jonxis JHP. The Hemoglobinopathies Techniques of Identification. Clinical and Biochemical Analysis, Vol. 6. New York: Marcel Dekker Inc., 1977.
  • Miller SA, Dykes DD, Polesky HF. A simple salting-out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988;16(3):1215.
  • Varawalla NY, Fitches AC, Old JM. Analysis of β-globin gene haplotypes in Asian Indians: origin and spread of β-thalassemia on the Indian subcontinent. Hum Genet. 1992;90(4):443–449.
  • Nagel RL. Disorders of hemoglobin function and stability. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL, Eds. Disorders of Hemoglobin. Genetics, Pathophysiology, and Clinical Management. Cambridge: Cambridge University Press. Cap. 44, 2005:1155–1194.
  • Hardison RC, Chui DHK, Giardine B, et al. HbVar: a relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat. 2002;19(3):225–233. http://globin.cse.psu.edu [].
  • Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537–541 http://globin.cse.psu.edu .
  • Magaña MT, Perea FJ, González JR, Ibarra B. Genetic relationship of a Mexican Afromestizo population through the analysis of the 3′ haplotype of the β globin gene in βA chromosomes. Blood Cells Mol Dis. 2007;39(2):169–177.

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.