Literature DB >> 28750473

A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX.

A Prabhudesai1, S Shanbhag1, D Mirgal1, N Kawankar1, S Shetty1.   

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Year:  2017        PMID： 28750473     DOI： 10.1111/hae.13307

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


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  1 in total

1.  Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis.

Authors:  Barbara Preisler; Behnaz Pezeshkpoor; Atanas Banchev; Ronald Fischer; Barbara Zieger; Ute Scholz; Heiko Rühl; Bettina Kemkes-Matthes; Ursula Schmitt; Antje Redlich; Sule Unal; Hans-Jürgen Laws; Martin Olivieri; Johannes Oldenburg; Anna Pavlova
Journal:  J Clin Med       Date:  2021-01-18       Impact factor: 4.241
  1 in total

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