Author: "Mälzer, M." / Database: Journals@OVID - Searchworks@Jio Institute Digital Library Search Results

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

Author: Brakensiek, K, Frye-Boukhriss, H, Mälzer, M, Abramowicz, M, Bahr, M J, von Beckerath, N, Bergmann, C, Caselitz, M, Holinski-Feder, E, Muschke, P, Oexle, K, Strobl-Wildemann, G, Wolff, G, El-Harith, E A, and Stuhrmann, M
Published: 2008

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