Pugliese, Alessia; Marina, Adela Della; Estephan, Eduardo de Paula; Zanoteli, Edmar 
; Roos, Andreas; Schara-Schmidt, Ulrike; Hentschel, Andreas; Azuma, Yoshiteru; Topf, Ana; Thompson, Rachel
Fonte: JOURNAL OF NEUROLOGY. Unidade: FM
Assuntos: DOENÇAS CONGÊNITAS, MIASTENIA GRAVIS, MUTAÇÃO GENÉTICA, DOENÇAS GENÉTICAS
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PUGLIESE, Alessia et al. Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case series. JOURNAL OF NEUROLOGY, v. 271, n. 3, p. 1331-1341, 2024Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/58924. Acesso em: 18 nov. 2024.APA
Pugliese, A., Marina, A. D., Estephan, E. de P., Zanoteli, E., Roos, A., Schara-Schmidt, U., et al. (2024). Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case series. JOURNAL OF NEUROLOGY, 271( 3), 1331-1341. doi:10.1007/s00415-023-12070-wNLM
Pugliese A, Marina AD, Estephan E de P, Zanoteli E, Roos A, Schara-Schmidt U, Hentschel A, Azuma Y, Topf A, Thompson R. Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case series [Internet]. JOURNAL OF NEUROLOGY. 2024 ; 271( 3): 1331-1341.[citado 2024 nov. 18 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58924Vancouver
Pugliese A, Marina AD, Estephan E de P, Zanoteli E, Roos A, Schara-Schmidt U, Hentschel A, Azuma Y, Topf A, Thompson R. Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case series [Internet]. JOURNAL OF NEUROLOGY. 2024 ; 271( 3): 1331-1341.[citado 2024 nov. 18 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58924
