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

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

PEDIATRIC NEPHROLOGY, cilt.39, sa.1, 2024 (SCI-Expanded, Scopus)

• Yayın Türü: Makale / Özet
• Cilt numarası: 39 Sayı: 1
• 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