von Willebrand factor A domain-containing protein 1 isoform 2 precurso - Protein

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Bi-allelic truncating mutations in VWA1 cause neuromyopathy. [Brain. 2021]
Bi-allelic truncating mutations in VWA1 cause neuromyopathy.
Deschauer M, Hengel H, Rupprich K, Kreiß M, Schlotter-Weigel B, Grimmel M, Admard J, Schneider I, Alhaddad B, Gazou A, et al. Brain. 2021 Mar 3; 144(2):574-583.
Immunocytochemical distribution of WARP (von Willebrand A domain-related protein) in the inner ear. [Brain Res. 2011]
Immunocytochemical distribution of WARP (von Willebrand A domain-related protein) in the inner ear.
Duong T, Lopez IA, Ishiyama A, Ishiyama G. Brain Res. 2011 Jan 7; 1367:50-61. Epub 2010 Nov 18.
Conformational stability and domain unfolding of the Von Willebrand factor A domains. [J Mol Biol. 2007]
Conformational stability and domain unfolding of the Von Willebrand factor A domains.
Auton M, Cruz MA, Moake J. J Mol Biol. 2007 Feb 23; 366(3):986-1000. Epub 2006 Oct 25.

RefSeq mRNA
See reference mRNA sequence for the VWA1 gene (NM_199121.3).
RefSeq protein isoforms
See the other reference sequence protein isoform for the VWA1 gene (NP_073745.2).

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