A novel KCNQ4 one-base deletion in a large pedigree with hearing loss : implication for the genotype-phenotype correlation

Author(s)

    • SUZUKI Yoichi
    • Department of Medical Genetics, Tohoku University School of Medicine
    • OSHIMA Takeshi
    • Department of Otorhinolaryngology, Head and Neck Surgery, Tohoku University School of Medicine
    • ICHINOHE Akiko
    • Department of Medical Genetics, Tohoku University School of Medicine
    • KOJIMA Kanako
    • Department of Medical Genetics, Tohoku University School of Medicine
    • NIIHORI Tetsuya
    • Department of Medical Genetics, Tohoku University School of Medicine
    • KANNO Junko
    • Department of Medical Genetics, Tohoku University School of Medicine
    • NARUMI Yoko
    • Department of Medical Genetics, Tohoku University School of Medicine
    • NARISAWA Ayumi
    • Department of Medical Genetics, Tohoku University School of Medicine
    • KATO Kumi
    • Department of Medical Genetics, Tohoku University School of Medicine
    • AOKI Yoko
    • Department of Medical Genetics, Tohoku University School of Medicine
    • IKEDA Katsuhisa
    • Department of Otorhinolaryngology, Head and Neck Surgery, Tohoku University School of Medicine
    • KOBAYASHI Toshimitsu
    • Department of Otorhinolaryngology, Head and Neck Surgery, Tohoku University School of Medicine

Journal

  • Journal of Human Genetics

    Journal of Human Genetics 51(5), 455-460, 2006-05-01

    Springer-Verlag Tokyo

References:  21

Cited by:  1

Codes

  • NII Article ID (NAID)
    10019168005
  • NII NACSIS-CAT ID (NCID)
    AA11206160
  • Text Lang
    ENG
  • Article Type
    Journal Article
  • ISSN
    14345161
  • NDL Article ID
    7909831
  • NDL Source Classification
    ZS16(科学技術--医学--人類遺伝学)
  • NDL Call No.
    Z54-H248
  • Data Source
    CJP  CJPref  NDL 
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