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Case Reports
. 2019 Aug;69(2):e55-e56.
doi: 10.1097/MPG.0000000000002306.

A Novel VPS33B Mutation Causing a Mild Phenotype of Arthrogryposis, Renal dysfunction, and Cholestasis Syndrome

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Case Reports

A Novel VPS33B Mutation Causing a Mild Phenotype of Arthrogryposis, Renal dysfunction, and Cholestasis Syndrome

Atu Agawu et al. J Pediatr Gastroenterol Nutr. 2019 Aug.
No abstract available

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