CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and rod myopathy due to a novel mutation in BTB domain of KBTBD13 gene presenting as LGMD.
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| Title: | CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and rod myopathy due to a novel mutation in BTB domain of KBTBD13 gene presenting as LGMD. |
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| Authors: | Garibaldi, M.1, Fattori, F.2, Bortolotti, C.3, Brochier, G.4, Labasse, C.4, Verardo, M.2, Bertini, E.2, Pennisi, E.5, Paradas, C.6, Romero, N.4, Antonini, G.1 |
| Source: | Neuromuscular Disorders. Oct2018:Supplement 2, Vol. 28, pS102-S102. 1p. |
| Database: | Academic Search Ultimate |
| ISSN: | 09608966 |
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| DOI: | 10.1016/j.nmd.2018.06.280 |
