When A Common Symptom of a Neonate Become an Unusual Diagnosis: A Case Report Of HMG-Coa Lyase Deficiency with a Novel Mutation
-
Published:2019-07-01
Issue:3
Volume:30
Page:
-
ISSN:2147-2092
-
Container-title:Gazi Medical Journal
-
language:
-
Short-container-title:GMJ
Publisher
Gazi University