When a common symptom of a neonate becomes an unusual diagnosis A case report of HMG CoA lyase deficiency


KASAPKARA Ç. S., AKAR M., BİBEROĞLU G., ÇELİK M., ÖZBEK M. N., TÜZÜN H.

Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Innsbruck, 2-5 September 2014., 2 - 05 September 2014, (Summary Text)

  • Publication Type: Conference Paper / Summary Text
  • Ankara Yıldırım Beyazıt University Affiliated: No