Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1.

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Welzel M., Akin L., Büscher A., Güran T., Hauffa B., Högler W., ...More

European journal of endocrinology, vol.168, pp.707-15, 2013 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 168
  • Publication Date: 2013
  • Doi Number: 10.1530/eje-12-1000
  • Title of Journal : European journal of endocrinology
  • Page Numbers: pp.707-15