Literature DB >> 16409483

A novel compound heterozygous mutation in the F13A gene causing hereditary factor XIII deficiency in a Chinese family.

S Wu, Z Wang, N Dong, X Bai, C Ruan.   

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Year:  2006        PMID： 16409483     DOI： 10.1111/j.1538-7836.2005.01699.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN： 1538-7836            Impact factor:   5.824


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  1 in total

1.  Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement.

Authors:  Siyu Ma; Changming Chen; Qian Liang; Xi Wu; Xuefeng Wang; Wenman Wu; Yan Liu; Qiulan Ding
Journal:  Orphanet J Rare Dis       Date:  2019-07-24       Impact factor: 4.123
  1 in total

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