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PCSK5 mutation in a patient with the VACTERL association.
Nakamura, Yukio; Kikugawa, Shingo; Seki, Shoji; Takahata, Masahiko; Iwasaki, Norimasa; Terai, Hidetomi; Matsubara, Mitsuhiro; Fujioka, Fumio; Inagaki, Hidehito; Kobayashi, Tatsuya; Kimura, Tomoatsu; Kurahashi, Hiroki; Kato, Hiroyuki.
Afiliación
  • Nakamura Y; Department of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Japan. yxn14@aol.jp.
  • Kikugawa S; DNA Chip Research Inc., Kanagawa, Japan. s-kikugawa@dna-chip.co.jp.
  • Seki S; Department of Orthopaedic Surgery, Faculty of Medicine, University of Toyama, Toyama, Japan. seki@med.u-toyama.ac.jp.
  • Takahata M; Department of Orthopaedic Surgery, Hokkaido University School of Medicine, Sapporo, Japan. takamasa@med.hokudai.ac.jp.
  • Iwasaki N; Department of Orthopaedic Surgery, Hokkaido University School of Medicine, Sapporo, Japan. niwasaki38@yahoo.co.jp.
  • Terai H; Department of Orthopaedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan. hterai@med.osaka-cu.ac.jp.
  • Matsubara M; Department of Orthopaedic Surgery, Nagano Prefectural Children's Hospital, Azumino, Japan. matsubara7942@yahoo.co.jp.
  • Fujioka F; Department of Orthopaedic Surgery, Nagano Prefectural Children's Hospital, Azumino, Japan. fujioka-fumio-r@pref-nagano-hosp.jp.
  • Inagaki H; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan. hinagaki@fujita-hu.ac.jp.
  • Kobayashi T; Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. tkobayashi1@partners.org.
  • Kimura T; Department of Orthopaedic Surgery, Faculty of Medicine, University of Toyama, Toyama, Japan. tkimura@med.u-toyama.ac.jp.
  • Kurahashi H; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan. kura@fujita-hu.ac.jp.
  • Kato H; Department of Orthopaedic Surgery, Shinshu University School of Medicine, Matsumoto, Japan. hirokato@shinshu-u.ac.jp.
BMC Res Notes ; 8: 228, 2015 Jun 09.
Article en En | MEDLINE | ID: mdl-26055999
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Canal Anal / Columna Vertebral / Tráquea / Mutación del Sistema de Lectura / Deformidades Congénitas de las Extremidades / Proproteína Convertasa 5 / Esófago / Cardiopatías Congénitas / Riñón Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Child / Humans / Male Idioma: En Revista: BMC Res Notes Año: 2015 Tipo del documento: Article País de afiliación: Japón
Texto completo
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PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Canal Anal / Columna Vertebral / Tráquea / Mutación del Sistema de Lectura / Deformidades Congénitas de las Extremidades / Proproteína Convertasa 5 / Esófago / Cardiopatías Congénitas / Riñón Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Child / Humans / Male Idioma: En Revista: BMC Res Notes Año: 2015 Tipo del documento: Article País de afiliación: Japón