G477 Identification of novel par2 mutation in thrombotic microangiopathy

P Walsh; R Asfahani; G Osman; D Hothi; A Waters

doi:10.1136/archdischild-2015-308599.431

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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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P Walsh 1Academic Renal Unit, University of Bristol, Bristol, UK2Institute of Child Health, University College London, London, UK PubMed articles Google scholar articles
R Asfahani 2Institute of Child Health, University College London, London, UK PubMed articles Google scholar articles
G Osman 2Institute of Child Health, University College London, London, UK PubMed articles Google scholar articles
D Hothi 3Renal Department, Great Ormond Street Hospital, London, UK PubMed articles Google scholar articles
A Waters 2Institute of Child Health, University College London, London, UK3Renal Department, Great Ormond Street Hospital, London, UK PubMed articles Google scholar articles

Citation

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.

Publication history

First published April 27, 2015.

Online issue publication

March 22, 2016

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