Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy

Autor: Coen A.C. Ottenheijm, Rhonda L. Taylor, Keren Muthsam, Gianina Ravenscroft, Gabrielle C. Musk, David J. Coote, Alison C. Testa, David Groth, Kristen J. Nowak, Elyshia McNamara, Amanda J. O'Hara, Nigel G. Laing, Joshua S. Clayton, James Kijas, Stefan Conijn, Hayley Goullee

Publikováno v: Acta neuropathologica communications, 8(1):142. BioMed Central
Clayton, J S, McNamara, E L, Goullee, H, Conijn, S, Muthsam, K, Musk, G C, Coote, D, Kijas, J, Testa, A C, Taylor, R L, O'Hara, A J, Groth, D, Ottenheijm, C A C, Ravenscroft, G, Laing, N G & Nowak, K J 2020, ' Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy ', Acta neuropathologica communications, vol. 8, no. 1, 142 . https://doi.org/10.1186/s40478-020-01017-1
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-14 (2020)

Ovine congenital progressive muscular dystrophy (OCPMD) was first described in Merino sheep flocks in Queensland and Western Australia in the 1960s and 1970s. The most prominent feature of the disease is a distinctive gait with stiffness of the hind

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https://research.vumc.nl/en/publications/0b321e4e-2c3a-4696-8c29-65820a916d08