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Corrigendum for McLean et al., Hum. Mol. Genet. 12 (18) 2395-2409.
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Human Molecular Genetics, 2004, Vol. 13, No. 3 365
DOI: 10.1093/hmg/ddh031

CORRIGENDUM

An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome

W. H. Irwin McLean, Alan D. Irvine, Kevin J. Hamill, Neil V. Whittock, Carrie M. Coleman-Campbell, Jemima E. Mellerio, Gabrielle S. Ashton, Patricia J. H. Dopping-Hepenstal, Robin A. J. Eady, Tanvir Jamil, Roderic J. Phillips, S. Ghulam Shabbir, Tahir S. Haroon, Khawar Khurshid, Jonathan E. Moore, Brian Page, Jonathan Darling, David J. Atherton, Maurice A. M. van Steensel, Colin S. Munro, Frances J. D. Smith and John A. McGrath

Human Molecular Genetics 12, 2395–2409 (2003)

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