X-linked recessive variants in X- Prolyl Aminopeptidase 2 ( XPNPEP2) as a potential new cause of nephrotic syndrome.


Mansour B., Schneider R., Franken G., Lemberg K., Yousef K., Frank C., ...Daha Fazla

PEDIATRIC NEPHROLOGY, sa.1, 2024 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Özet
  • Basım Tarihi: 2024
  • Dergi Adı: PEDIATRIC NEPHROLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, CINAHL, MEDLINE, Veterinary Science Database
  • Gazi Üniversitesi Adresli: Evet