Variant late-infantile neuronal ceroid lipofuscinosis due to a novel heterozygous CLN8 mutation and de novo 8p23.3 deletion

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

Original languageEnglish (Ireland)
JournalClin Genetclin Genet
Volume81
Issue number66
Publication statusPublished - 1 Jun 2012

Authors (Note for portal: view the doc link for the full list of authors)

  • Authors
  • Allen, N. M.,O'HIci, B.,Anderson, G.,Nestor, T.,Lynch, S. A.,King, M. D.

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