Volume 105, Issue 3 pp. 670-672

Prothrombin Carora: hypoprothrombinaemia caused by substitution of Tyr-44 by Cys

William Y. Sun

William Y. Sun

Banco Municipal de Sangre del Distrito Federal, Caracas, Venezuela

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Arlette Ruiz-Saez

Arlette Ruiz-Saez

Division of Developmental Biology, Children's Hospital Research Foundation, Cincinnati, Ohio,

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Melissa C. Burkart

Melissa C. Burkart

Banco Municipal de Sangre del Distrito Federal, Caracas, Venezuela

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Norma Bosch

Norma Bosch

Division of Developmental Biology, Children's Hospital Research Foundation, Cincinnati, Ohio,

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Sandra J. F. Degen

Sandra J. F. Degen

Division of Developmental Biology, Children's Hospital Research Foundation, Cincinnati, Ohio,

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First published: 25 December 2001
Citations: 6
Sandra J. F. Degen, Division of Developmental Biology, Children's Hospital Research Foundation, 3333 Burnet Avenue, Cincinnati, OH 45229, U.S.A. e-mail: [email protected]

Abstract

Two members of a family from Carora, Venezuela, were found to have prothrombin activity levels at 4% of normal and undetectable antigen levels. All exons of the prothrombin gene from the proband were sequenced and a mutation at nucleotide 1305 was identified that would result in the substitution of Cys for Tyr at residue 44. Residue 44 is present in the aromatic stack region of the protein. Substitution of a Cys in this region would result in an abnormal folding of the protein which could be the cause for the observed lack of secretion of the abnormal prothrombin.

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