Homozygous delayed initiation codon mutation in the laminin A3A isoform causes LOC syndrome

I McLean, K J Hamill, F J D Smith, N V Whitlock, C S Coleman, R A J Eady, C S Munro, A D Irvine, T Jamil, J McGrath

Research output: Contribution to journalMeeting abstract

Original languageEnglish
Pages (from-to)S20 - S20
JournalJournal of Medical Genetics
Volume40
Publication statusPublished - 2003
EventBritish Human Genetics Conference - YORK, ENGLAND, United Kingdom
Duration: 15 Sept 200317 Sept 2003

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