Shaw‐Smith, C., & Grulich-Henn, J. (2012). Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia. Pediatric diabetes, 13(4), . https://doi.org/10.1111/j.1399-5448.2012.00855.x
Chicago-Zitierstil (17. Ausg.)Shaw‐Smith, Charles, und Jürgen Grulich-Henn. "Recessive SLC19A2 Mutations Are a Cause of Neonatal Diabetes Mellitus in Thiamine-responsive Megaloblastic Anaemia." Pediatric Diabetes 13, no. 4 (2012). https://doi.org/10.1111/j.1399-5448.2012.00855.x.
MLA-Zitierstil (9. Ausg.)Shaw‐Smith, Charles, und Jürgen Grulich-Henn. "Recessive SLC19A2 Mutations Are a Cause of Neonatal Diabetes Mellitus in Thiamine-responsive Megaloblastic Anaemia." Pediatric Diabetes, vol. 13, no. 4, 2012, https://doi.org/10.1111/j.1399-5448.2012.00855.x.