Source: Acta neuropathologica. Unidade: FM
Subjects: MIOPATIAS CONGÊNITAS ESTRUTURAIS, MUTAÇÃO GENÉTICA, DIAGNÓSTICO, DOENÇAS CONGÊNITAS
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BIANCALANA, Valérie e ZANOTELI, Edmar. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues. Acta neuropathologica, v. 134, p. 889-904, 2017Tradução . . Disponível em: https://doi.org/10.1007/s00401-017-1748-0. Acesso em: 04 nov. 2024.APA
Biancalana, V., & Zanoteli, E. (2017). Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues. Acta neuropathologica, 134, 889-904. doi:10.1007/s00401-017-1748-0NLM
Biancalana V, Zanoteli E. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues [Internet]. Acta neuropathologica. 2017 ; 134 889-904.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s00401-017-1748-0Vancouver
Biancalana V, Zanoteli E. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues [Internet]. Acta neuropathologica. 2017 ; 134 889-904.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s00401-017-1748-0
