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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

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