Literature DB >> 10477436

Deep intronic mutations are rarely a cause of hemophilia B.

J Feng, Q Liu, J Drost, S S Sommer.   

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Year:  1999        PMID： 10477436     DOI： 10.1002/(SICI)1098-1004(1999)14:3<267::AID-HUMU11>3.0.CO;2-I

Source DB:  PubMed          Journal:  Hum Mutat        ISSN： 1059-7794            Impact factor:   4.878


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  2 in total

1.  Enhanced carrier and prenatal diagnosis in the Italian haemophilia B population.

Authors:  Anne Goodeve
Journal:  Blood Transfus       Date:  2007-07       Impact factor: 3.443

Review 2.  Hemophilia B: molecular pathogenesis and mutation analysis.

Authors:  A C Goodeve
Journal:  J Thromb Haemost       Date:  2015-05-18       Impact factor: 5.824
  2 in total

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