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Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss

RepositoryUniversity of Melbourne [Minerva Access]
URLhttp://hdl.handle.net/11343/219698
Author(s)orcid:0000-0001-6049-6931; orcid:0000-0002-8847-9401; orcid:0000-0001-6397-1910; orcid:0000-0001-7191-8511; orcid:0000-0001-5132-0774; orcid:0000-0003-2531-8413; Marsh, APL; Lukic, V; Pope, K; Bromhead, C; Tankard, R; Ryan, MM; Yiu, EM; Sim, JCH; Delaryck
Item typeArticle
JournalNeurology Genetics, Print_ISSN:2376-7839, Online_ISSN:2376-7839
DOIhttps://doi.org/10.1212/NXG.0000000000000014

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