ARRANZ Jose | Unitat de Metabolopaties, Hospital Universitari Materno-Infantil Vall d'Hebron, Passeig de la Vall d'Hebron

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概要

• 同名の論文著者
• Unitat de Metabolopaties, Hospital Universitari Materno-Infantil Vall d'Hebron, Passeig de la Vall d'Hebronの論文著者

関連著者

• Yoshino Makoto

  久留米大学 医学部小児科学

• Numata Sanae

  Department Of Pediatrics And Child Health Kurume University School Of Medicine

• Maruyama Yoshio

  Department Of Physiology Tohoku University Graduate School Of Medicine

• Yoshino Makoto

  Department Of Advanced Materials Science & Engineering Faculty Of Engineering Yamaguchi Universi

• Endo Fumio

  Department O Pediatrics Graduate School Of Medical Science Kumamoto University

• Ihara Kenji

  Department Of Pediatrics Graduate School Of Medical Science Kyushu University

• Okano Yoshiyuki

  Department Of Pediatrics Osaka City University Graduate School Of Medicine

• Sawada Tomo

  Department Of Pediatrics Osaka City University Graduate School Of Medicine

• Koda Yoshiro

  Department Of Forensic Medicine And Human Genetics Kurume University School Of Medicine

• Matsuura Toshinobu

  Department Of Pediatrics Kumamoto University Medical School

• Yoo Han-wook

  Department Of Pediatrics Asan Medical Center Children's Hospital University Of Ulsan College Of

• Endo Fumio

  Department Of Pediatrics Graduate School Of Medicine Kumamoto University

• ARRANZ Jose

  Unitat de Metabolopaties, Hospital Universitari Materno-Infantil Vall d'Hebron, Passeig de la Vall d'Hebron

• RUBIO Vicente

  Instituto de Biomedicina de Valencia (IBV-CSIC) and CIBERER-ISCIII

• WERMUTH Bendicht

  Universitatsinstitut fur Klinische Chemie/Molekulare Diagnostik

• MEW Nicholas

  Children's National Medical Center

• TUCHMAN Mendel

  Children's National Medical Center

• PINNER Jason

  Department of Medical Genetics, Sydney Children's Hospital

• KIRK Edwin

  Department of Medical Genetics, Sydney Children's Hospital

• Kirk Edwin

  Department Of Medical Genetics Sydney Children's Hospital

• Mew Nicholas

  Children's National Medical Center

• Tuchman Mendel

  Children's National Medical Center

• Yoo Han-wook

  Department Of Pediatrics Asan Medical Center

• Matsuura Toshinobu

  Department Of Pediatrics Graduate School Of Medicine Kumamoto University

• Arranz Jose

  Unitat De Metabolopaties Hospital Universitari Materno-infantil Vall D'hebron Passeig De La Vall D'hebron

• Okano Yoshiyuki

  Department Of Pediatrics Osaka City Graduate School Of Medicine

• PINNER Jason

  Department of Medical Genetics, Sydney Children's Hospital

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著作論文

• Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations

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