Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities

समान संसाधन

• Imerslund-Gräsbeck syndrome: a comprehensive review of reported cases
  द्वारा: Sandra D.K. Kingma, और अन्य
  प्रकाशित: (2023-09-01)
• Severe pancytopenia at the presentation of Imerslund-Gräsbeck syndrome in a 23-month-old Italian boy
  द्वारा: Francesca Di Sario, और अन्य
  प्रकाशित: (2024-09-01)
• Profound vitamin D deficiency in four siblings with Imerslund‐Grasbeck syndrome with homozygous CUBN mutation
  द्वारा: Jose I. R. Ciancio, और अन्य
  प्रकाशित: (2019-09-01)
• Imerslund-Gräsbeck syndrome in a child with a novel compound heterozygous mutations in the AMN gene: a case report
  द्वारा: Dedong Zhang, और अन्य
  प्रकाशित: (2024-09-01)
• A child with Imerslund-Gräsbeck syndrome concealed by co‐existing α-thalassaemia presenting with subacute combined degeneration of the spinal cord: a case report
  द्वारा: Visvalingam Arunath, और अन्य
  प्रकाशित: (2021-01-01)