Pediatric Neurology
Volume 26, Issue 1 , Pages 65-67, January 2002

A novel mutation, P126R, in a Japanese patient with HHH syndrome

  • Takeshi Miyamoto, MD

      Affiliations

    • Department of Inherited Metabolic Disease, National Institute of Neuroscience, NCNP, Tokyo, Japan
    • ,
  • Naomi Kanazawa, BS

      Affiliations

    • Department of Inherited Metabolic Disease, National Institute of Neuroscience, NCNP, Tokyo, Japan
    • Research Division of Biochemistry, Kitasato University School of Medicine, Kanagawa, Japan
    • ,
  • Chiemi Hayakawa, MD

      Affiliations

    • Department of Pediatrics, Central Hospital, Aichi Welfare Center for Persons with Developmental Disabilities, Aichi, Japan
    • ,
  • Seiichi Tsujino, MD

      Affiliations

    • Corresponding Author InformationCommunications should be addressed to: Dr. Tsujino; Department of Inherited Metabolic Disease; National Institute of Neuroscience; NCNP; 4-1-1, Ogawahigashi; Kodaira; Tokyo 187-8502 Japan
    • Department of Inherited Metabolic Disease, National Institute of Neuroscience, NCNP, Tokyo, Japan

Received 5 April 2001; accepted 27 June 2001.

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PII: S0887-8994(01)00335-6

Pediatric Neurology
Volume 26, Issue 1 , Pages 65-67, January 2002

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