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 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 168
  • Publication Date: 2013
  • Doi Number: 10.1530/eje-12-1000
  • Journal Name: European journal of endocrinology
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.707-15
  • Kütahya Health Sciences University Affiliated: No