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A COL4A1 variant in a neonate with multiple intracranial hemorrhages and congenital cataracts.
Yakabe, Ayane; Ikuse, Tamaki; Ito, Natsuki; Yamada, Hiromichi; Saito, Nobutomo; Kitamura, Yuri; Iwasaki, Tomohiro; Ikeno, Mitsuru; Suganuma, Hiroki; Abe, Shinpei; Miyazaki, Nao; Hisata, Ken; Shoji, Hiromichi; Nakazawa, Tomoyuki; Eguchi, Hidetaka; Shimizu, Toshiaki.
Afiliación
  • Yakabe A; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Ikuse T; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan. taikuse@juntendo.ac.jp.
  • Ito N; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Yamada H; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Saito N; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Kitamura Y; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Iwasaki T; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Ikeno M; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Suganuma H; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Abe S; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Miyazaki N; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Hisata K; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Shoji H; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Nakazawa T; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
  • Eguchi H; Diagnostics and Therapeutics of Intractable Diseases and Intractable Disease Research Center, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Shimizu T; Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
Hum Genome Var ; 9(1): 24, 2022 Jun 10.
Article en En | MEDLINE | ID: mdl-35688819
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Hum Genome Var Año: 2022 Tipo del documento: Article País de afiliación: Japón
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Hum Genome Var Año: 2022 Tipo del documento: Article País de afiliación: Japón