A Novel SMAD4 Mutation Causing Severe Juvenile Polyposis Syndrome with Protein Losing Enteropathy, Immunodeficiency, and Hereditary Haemorrhagic Telangiectasia.
Autor: | Johansson, Joel1 joejo597@student.liu.se, Sahin, Christofer1 chrsa265@student.liu.se, Pestoff, Rebecka2 rebecka.pestoff@lio.se, Ignatova, Simone2 simone.ignatova@lio.se, Forsberg, Pia3 pia.forsberg@liu.se, Edsjö, Anders4 anders.edsjo@gu.se, Ekstedt, Mattias1 mattias.ekstedt@lio.se, Stenmark Askmalm, Marie2 mariestenmark@icloud.com |
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Zdroj: | Case Reports in Gastrointestinal Medicine. 2/1/2015, Vol. 2015, p1-5. 5p. |
Databáze: | Academic Search Ultimate |
Externí odkaz: |