Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

AYCAN Z., Savas-Erdeve S., Cetinkaya S., Kurnaz E., Keskin M., Sahin N. M., ...Daha Fazla

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.10, sa.3, ss.223-229, 2018 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 10 Sayı: 3
  • Basım Tarihi: 2018
  • Doi Numarası: 10.4274/jcrpe.5506
  • Dergi Adı: JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.223-229
  • Anahtar Kelimeler: MKRN3 mutation, familial central precocious puberty, genetic analysis, IMPRINTED GENE MKRN3, GIRLS, CHILDREN, PATTERN
  • Ankara Üniversitesi Adresli: Hayır

Özet

Objective: There have been recent advances in the understanding of the etiology of idiopathic central precocious puberty (iCPP) including new genetic associations. The aim of this clinical study was to determine the frequency of MKRN3 mutation in cases of familial iCPP.