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Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia

✍ Scribed by K Brakensiek; H Frye-Boukhriss; M Mälzer; M Abramowicz; MJ Bahr; N Von Beckerath; C Bergmann; M Caselitz; E Holinski-Feder; P Muschke; K Oexle; G Strobl-Wildemann; G Wolff; EA El-Harith; M Stuhrmann

Book ID: 110888631
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 103 KB
Volume: 74
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.2008.01029.x

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