Genetic variants of transferrin in cystic fibrosis
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-008-0733-0
Reference15 articles.
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2. Beckman LE, Van Landeghem GF, Sikstrom C, Beckman L (1998) DNA polymorphisms and haplotypes in the human transferrin gene. Hum Genet 102: 141–144.
3. Du Chesne A (1993) Does the transferrin C2 frequency depend on age? Hum Hered 43: 63–65.
4. Kamboh MI, Ferrell RE (1987) Human transferrin polymorphism (review). Hum Hered 37: 65–81.
5. Kühnl P, Spielmann W, Weber W (1979) Isoelectric focusing of rare transferrin (Tf) variants and common TfC subtypes. Hum Genet 46(1): 83–87.
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1. Breakthrough Varicella Zoster Virus Infection in an Immunized Child with Cystic Fibrosis;Pediatric Infectious Disease Journal;2016-05
2. A novel mutation on the transferrin gene abolishes one N-glycosylation site and alters the pattern of transferrin isoforms, mimicking that observed after excessive alcohol consumption;Clinical Biochemistry;2016-04
3. Determination of genetic transferrin variants in human serum by high-resolution capillary zone electrophoresis†;Journal of Separation Science;2014-05-16
4. No association of TF gene polymorphisms with hepatitis B virus Clearance and hepatocellular carcinoma occurrence in a Korean population;Genes & Genomics;2011-06
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