Literature DB >> 17498086

Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment.

J Ingerslev, T Herlin, B Sørensen, N Clausen, K C Chu, K A High.   

Abstract

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Year:  2007        PMID： 17498086     DOI： 10.1111/j.1365-2516.2007.01466.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN： 1351-8216            Impact factor:   4.287


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  1 in total

1.  Characterization of a Missense Mutation in the Catalytic Domain and a Splicing Mutation of Coagulation Factor X Compound Heterozygous in a Chinese Pedigree.

Authors:  Yuanzheng Feng; Jiewen Ma; Liang V Tang; Wenyi Lin; Yanyi Tao; Zhipeng Cheng; Yu Hu
Journal:  Genes (Basel)       Date:  2021-09-27       Impact factor: 4.096
  1 in total

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