Kinesin family member 12 ‐related hepatopathy: A generally indolent disorder with elevated gamma‐glutamyl‐transferase activity

Documenti analoghi

• Deep‐Intronic Variant in RUNX2 Causing Pseudo‐Exon Inclusion in a Family With Cleidocranial Dysplasia
  di: Dorothea Stojanovic, et al.
  Pubblicazione: (2026)
• Pathogenic Deep Intronic PCSK1 Variant Causes Proprotein Convertase 1/3 Deficiency in a Family
  di: Leah M. Huber, et al.
  Pubblicazione: (2025)
• Gamma‐glutamyl transferase and the risk of all‐cause and disease‐specific mortality in patients with diabetes: A nationwide cohort study
  di: Goh Eun Chung, et al.
  Pubblicazione: (2024)
• Re‐engineering a transferase scaffold for indole C3 methylation in diketopiperazines
  di: Mona Haase, et al.
  Pubblicazione: (2025)
• Gamma‐glutamyl transferase: A potential biomarker for pancreas steatosis in patients with concurrent obesity, insulin resistance and metabolic dysfunction‐associated steatotic liver disease
  di: Chileka Chiyanika, et al.
  Pubblicazione: (2024)