G477 Identification of novel par2 mutation in thrombotic microangiopathy | Archives of Disease in Childhood

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British Society for Paediatric Endocrinology and Diabetes and British Association for Paediatric Nephrology

G477 Identification of novel par2 mutation in thrombotic microangiopathy

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Cite this article as:: Walsh P, Asfahani R, Osman G, et al

G477 Identification of novel par2 mutation in thrombotic microangiopathy

Archives of Disease in Childhood 2015;100:A203-A204.