Complete exon–intron organization of the gene for human lysyl hydroxylase 3 (LH3)

This publication has 21 references indexed in Scilit:

• Cloning and characterization of a third human lysyl hydroxylase isoform
  Proceedings of the National Academy of Sciences, 1998
• Ehlers-Danlos syndrome type VI: lysyl hydroxylase deficiency due to a novel point mutation (W612C)
  Archives of Dermatological Research, 1998
• The Serotonin 1a Receptor Gene Contains a TATA-less Promoter that Responds to MAZ and Sp1
  Journal of Biological Chemistry, 1996
• Structure and Expression of the Human Lysyl Hydroxylase Gene (PLOD): Introns 9 and 16 Contain Alu Sequences at the Sites of Recombination in Ehlers-Danlos Syndrome Type VI Patients
  Genomics, 1994
• A patient with Ehlers-Danlos syndrome type VI is a compound heterozygote for mutations in the lysyl hydroxylase gene.
  Journal of Clinical Investigation, 1994
• DNA sequence requirements for transcriptional initiator activity in mammalian cells.
  Molecular and Cellular Biology, 1994
• A Large Duplication in the Gene for Lysyl Hydroxylase Accounts for the Type VI Variant of Ehlers-Danlos Syndrome in Two Siblings
  Genomics, 1993
• A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers–Danlos syndrome type VI
  Nature Genetics, 1992
• Cloning of human lysyl hydroxylase: Complete cDNA-derived amino acid sequence and assignment of the gene (PLOD) to chromosome 1p36.3→p36.2
  Genomics, 1992
• Characterization of a Pro-α2(I) collagen gene mutation by nuclease S1 mapping
  Published by Elsevier ,1987