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Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy.
Kuroha, Yasuko; Ishiguro, Takanobu; Tada, Mari; Hara, Norikazu; Murayama, Kei; Kawachi, Izumi; Kasuga, Kensaku; Miyashita, Akinori; Hasegawa, Arika; Takahashi, Tetsuya; Matsubara, Nae; Onodera, Osamu; Kakita, Akiyoshi; Koike, Ryoko; Ikeuchi, Takeshi.
Afiliação
  • Kuroha Y; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Ishiguro T; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Tada M; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Hara N; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Murayama K; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Kawachi I; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Kasuga K; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Miyashita A; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Hasegawa A; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Takahashi T; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Matsubara N; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Onodera O; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Kakita A; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Koike R; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
  • Ikeuchi T; Department of Neurology (Y.K., A.H., T.T., N.M., R.K.), Nishiniigata Chuo Hospital, Niigata; Department of Molecular Genetics (Y.K., T. Ishiguro, N.H., K.K., A.M., T. Ikeuchi), Department of Neurology (T. Ishiguro, I.K., O.O.), and Department of Pathology (M.T., A.K.), Brain Research Institute, Niig
Neurol Genet ; 8(5): e200030, 2022 Oct.
Article em En | MEDLINE | ID: mdl-36176336

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Neurol Genet Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Neurol Genet Ano de publicação: 2022 Tipo de documento: Article
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