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Adult-onset leukoencephalopathy with homozygous LAMB1 missense mutation.
Yasuda, Rei; Yoshida, Tomokatsu; Mizuta, Ikuko; Watanabe, Masashi; Nakano, Masakazu; Sato, Ryuichi; Tokuda, Yuichi; Omi, Natsue; Sakai, Norio; Nakagawa, Masanori; Tashiro, Kei; Mizuno, Toshiki.
Afiliación
  • Yasuda R; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Yoshida T; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Mizuta I; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Watanabe M; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Nakano M; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Sato R; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Tokuda Y; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Omi N; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Sakai N; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Nakagawa M; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Tashiro K; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
  • Mizuno T; Department of Neurology (R.Y., T.Y., I.M., T.M.), Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Neurology (M.W.), Ehime Prefectural Central Hospital, Ehime, Japan; Department of Genomic Medical Sciences (M. Nakano, R.S., Y.T., N.O., K.T.),
Neurol Genet ; 6(4): e442, 2020 Aug.
Article en En | MEDLINE | ID: mdl-32548278

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Neurol Genet Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Neurol Genet Año: 2020 Tipo del documento: Article