Heterozygous CAPN3 missense variants causing autosomal‐dominant calpainopathy in seven unrelated families.

Autor: González‐Mera, L.1,2 (AUTHOR), Ravenscroft, G.3 (AUTHOR), Cabrera‐Serrano, M.3,4,5,6 (AUTHOR), Ermolova, N.7 (AUTHOR), Domínguez‐González, C.8 (AUTHOR), Arteche‐López, A.9 (AUTHOR), Soltanzadeh, P.10 (AUTHOR), Evesson, F.11,12 (AUTHOR), Navas, C.1 (AUTHOR), Mavillard, F.5,6 (AUTHOR), Clayton, J.3 (AUTHOR), Rodrigo, P.1,2 (AUTHOR), Servián‐Morilla, E.4,5,6 (AUTHOR), Cooper, S. T11,12,13 (AUTHOR), Waddell, L.11,13 (AUTHOR), Reardon, K.14 (AUTHOR), Corbett, A.15 (AUTHOR), Hernandez‐Laín, A.16 (AUTHOR), Sanchez, A.17 (AUTHOR), Esteban Perez, J.8 (AUTHOR)
Zdroj: Neuropathology & Applied Neurobiology. Feb2021, Vol. 47 Issue 2, p283-296. 14p.
Databáze: Academic Search Ultimate
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