Mutation analysis of Swedish haemophilia B families – high frequency of unique mutations-Reference-Cited by-同舟云学术

Mutation analysis of Swedish haemophilia B families – high frequency of unique mutations

Author:

Mårtensson A.¹²,Letelier A.¹²,Halldén C.³,Ljung R.¹²

Affiliation:

1. Department of Clinical Sciences Lund University Malmö Sweden

2. Department of Paediatrics and Malmö Centre for Thrombosis and Haemostasis Skåne University Hospital Lund University Malmö Sweden

3. Biomedicine Kristianstad University Kristianstad Sweden

Funder

Lunds Universitet

Vetenskapsrådet

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

Reference35 articles.

3. Royal Free London NHS Foundation Trust.Factor IX variant database.London UK 2012. Available atwww.factorix.org. Accessed August 6 2015.

5. Centers for Disease Control and Prevention.CHBMP F9 mutation list.2015. Available atwww.cdc.gov/hemophiliamutations. Accessed August 6 2015.

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