Related Articles
Clinical and molecular study of a pediatric patient with sodium taurocholate cotransporting polypeptide deficiency
Identification of novel mutations of the HADHA and HADHB genes in patients with mitochondrial trifunctional protein deficiency
Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China
Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non‑syndromic hearing loss
Successful allogeneic hematopoietic stem cell transplantation in a boy with X-linked inhibitor of apoptosis deficiency presenting with hemophagocytic lymphohistiocytosis: A case report