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A Novel Nonsense Mutation in the EDA Gene Causing X-Linked Hypohidrotic Ectodermal Dysplasia

Author

Listed:
  • Liu Guannan

    (Peking University School and Hospital of Stomatology, Department of Pediatric Dentistry
    Peking University International Hospital, Department of Stomatology)

  • Wang Xin
  • Qin Man
  • Zhu Junxia

    (Peking University School and Hospital of Stomatology, Department of Pediatric Dentistry)

  • Sun Lisha

    (Peking University School and Hospital of Stomatology, Central Laboratory)

Abstract

X-linked hypohidrotic ectodermal dysplasia (XLHED) can be characterized by hypohidrosis, sparse hair, hypodontia, and characteristic facial features and usually caused by mutations of ectodysplasin A (EDA) gene located on the X chromosome.

Suggested Citation

  • Liu Guannan & Wang Xin & Qin Man & Zhu Junxia & Sun Lisha, 2018. "A Novel Nonsense Mutation in the EDA Gene Causing X-Linked Hypohidrotic Ectodermal Dysplasia," Biomedical Journal of Scientific & Technical Research, Biomedical Research Network+, LLC, vol. 12(3), pages 1-4, December.
  • Handle: RePEc:abf:journl:v:12:y:2018:i:3:p:1-4
    DOI: 10.26717/BJSTR.2018.12.002249
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    More about this item

    Keywords

    Biomedical Sciences; Biomedical Research; Technical research; Etodysplasin A; Hypohidrotic Ectodermal Dysplasia; Mutation; Nonsense;
    All these keywords.

    JEL classification:

    • R00 - Urban, Rural, Regional, Real Estate, and Transportation Economics - - General - - - General
    • Z0 - Other Special Topics - - General

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