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Clinical Genetics|May 24, 2008
Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasiaK Brakensiek, H Frye-Boukhriss, M Mälzer, et al.
Structure (London, England : 1993)|March 27, 2018
An Intracellular Allosteric Modulator Binding Pocket in SK2 Ion Channels Is Shared by Multiple ChemotypesLily T-Y Cho, Aristos J Alexandrou, Rubben Torella, et al.
Genetics in Medicine Open|December 13, 2024
ARID1B-related disorder in 87 adults: Natural history and self-sustainabilityP J van der Sluijs, M Gösgens, A J M Dingemans, et al.
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