Related Articles
X‑linked adrenoleukodystrophy caused by maternal ABCD1 mutation and paternal X chromosome inactivation
Analysis of hepatitis B virus genotype and gene mutation in patients with advanced liver disease in East Kalimantan, Indonesia
Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta
A novel NHS mutation in a Chinese family with Nance‑Horan Syndrome
Successful allogeneic hematopoietic stem cell transplantation in a boy with X-linked inhibitor of apoptosis deficiency presenting with hemophagocytic lymphohistiocytosis: A case report