Transferrin Variants in Japan and New Zealand-Reference-Cited by-同舟云学术

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Transferrin Variants in Japan and New Zealand

Published:1987 Issue:1 Volume:37 Page:20-25
ISSN:1423-0062
Container-title:Human Heredity
language:en
Short-container-title:Hum Hered

Author:

Yuasa I.,Saneshige Y.,Suenaga S.,Ito K.,Gotoh Y.

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I;Journal of Inherited Metabolic Disease;2011-03-23

2. Transferrin D protein variants in the diagnosis of congenital disorders of glycosylation (CDG);Journal of Clinical Laboratory Analysis;2009

3. Determination of carbohydrate-deficient transferrin separated by lectin affinity chromatography for detecting chronic alcohol abuse;FEBS Letters;1999-09-10

4. Subtyping of transferrin by isoelectric focusing in immobilized pH gradients;Electrophoresis;1998-06

5. Transferrin Polymorphism in the Nansei Islands: Description of a New Variant TF Dama and Clines of Allele Frequencies in Japanese Populations.;Anthropological Science;1998

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