Correction: Novel SLC16A2 mutations in patients with Allan-Herndon-Dudley syndrome

Benzer Materyaller

• Novel SLC16A2 mutations in patients with Allan-Herndon-Dudley syndrome
  Yazar:: Shimojima, Keiko, ve diğerleri
  Baskı/Yayın Bilgisi: (2016)
• SLC16A2 mutations in two Japanese patients with Allan–Herndon–Dudley syndrome
  Yazar:: Yamamoto, Toshiyuki, ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Novel SLC16A2 Frameshift Mutation as a Cause of Allan-Herndon-Dudley Syndrome and its Implications for Carrier Screening
  Yazar:: Lin P, ve diğerleri
  Baskı/Yayın Bilgisi: (2025-04-01)
• A Novel Deletion Mutation of SLC16A2 Encoding Monocarboxylate Transporter (MCT) 8 in a 26-year-old Japanese Patient with Allan-Herndon-Dudley Syndrome
  Yazar:: Yamamoto, Sayaka, ve diğerleri
  Baskı/Yayın Bilgisi: (2013)
• Allan-Herndon-Dudley syndrome in a female patient and related mechanisms
  Yazar:: Caroline Olivati, ve diğerleri
  Baskı/Yayın Bilgisi: (2022-06-01)