Associated Papers
A novel homozygous splice-site variant in VPS33B identified as a cause of bleeding.
Díaz-Ajenjo L et al.
Journal of Thrombosis and Haemostasis : Jth, 2026
Arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome: from molecular genetics to clinical features.
Zhou Y et al.
Italian Journal of Pediatrics, 2014
[The progress in molecular genetics and clinical features of arthrogryposis-renal tubular dysfunction-cholestasis syndrome].
Lan T et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2014
Clinical and molecular genetic features of ARC syndrome.
Gissen P et al.
Human Genetics, 2006
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