Molecular characterization of a third case of human atransferrinemia-Reference-Cited by-同舟云学术

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Molecular characterization of a third case of human atransferrinemia

Published:2004-10-15 Issue:8 Volume:104 Page:2607-2607
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Knisely A.S.,Gelbart Terri,Beutler Ernest

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/104/8/2607/1702665/zh802004002607a.pdf

Reference12 articles.

1. Beutler E, Gelbart T, Lee P, Trevino R, Fernandez MA, Fairbanks VF. Molecular characterization of a case of atransferrinemia. Blood. 2000;96: 4071-4074.

2. Stavem P, Saltvedt E, Elgjo K, Rootwelt K. Congenital hypochromic microcytic anaemia with iron overload of the liver and hyperferraemia. Scand J Haematol. 1973;10: 153-160.

3. Trenor CC, Campagna DR, Sellers VM, Andrews NC, Fleming MD. The molecular defect in hypotransferrinemic mice. Blood. 2000;96: 1113-1118.

4. Antonarakis SE. Recommendations for a nomenclature system for human gene mutations: Nomenclature Working Group. Hum Mutat. 1998;11: 1-3.

5. den Dunnen JT, Antonarakis SE. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat. 2000;15: 7-12.

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