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

Amri, Yessine; Dabboubi, Rym; Mghaieth, Fathia; Zili, Mohamed; Messaoud, Taieb; Casini, Alessandro; De Moerloose, Philippe; Toumi, Nour El Houda

doi:10.1111/hae.13974

Scientific article

Letter

English

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

ContributorsAmri, Yessine; Dabboubi, Rym; Mghaieth, Fathia; Zili, Mohamed; Messaoud, Taieb; Casini, Alessandro

; De Moerloose, Philippe; Toumi, Nour El Houda

Published inHaemophilia

Publication date2020

Affiliation entities

Faculté de médecine / Section de médecine clinique / Département de médecine

Research groups

Citation (ISO format)

AMRI, Yessine et al. Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion. In: Haemophilia, 2020. doi: 10.1111/hae.13974

Article (Published version)

Identifiers

PID : unige:135207
DOI : 10.1111/hae.13974
PMID : 32202028

Additional URL for this publicationhttps://onlinelibrary.wiley.com/doi/full/10.1111/hae.13974

Journal ISSN1351-8216

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Creation18/04/2020 08:24:00

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

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