Literature DB >> 32202028

Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion.

Yessine Amri1, Rym Dabboubi1, Fathia Mghaieth2, Mohamed Zili3, Taieb Messaoud1, Alessandro Casini4, Philippe De Moerloose4, Nour El Houda Toumi5,6.   

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Year:  2020        PMID： 32202028     DOI： 10.1111/hae.13974

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


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  1 in total

Review 1.  Heterogeneity of Genotype-Phenotype in Congenital Hypofibrinogenemia-A Review of Case Reports Associated with Bleeding and Thrombosis.

Authors:  Monika Brunclikova; Tomas Simurda; Jana Zolkova; Miroslava Sterankova; Ingrid Skornova; Miroslava Dobrotova; Zuzana Kolkova; Dusan Loderer; Marian Grendar; Jan Hudecek; Jan Stasko; Peter Kubisz
Journal:  J Clin Med       Date:  2022-02-18       Impact factor: 4.241
  1 in total

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