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Homozygous delayed initiation codon mutation in the laminin A3A isoform causes LOC syndrome
Homozygous delayed initiation codon mutation in the laminin A3A isoform causes LOC syndrome
2003
Irwin McLean
Kevin J. Hamill
F.J.D. Smith
N V Whitlock
Carrie S. Coleman
Robin A.J. Eady
Colin S. Munro
Alan D. Irvine
T. Jamil
J.C. McGrath
Keywords:
Gene isoform
Genetics
Laminin
LOC syndrome
Start codon
Biology
Mutation
Molecular biology
Correction
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