Organization and Nucleotide Sequence of the Human Hermansky-Pudlak Syndrome (HPS) Gene
- 1 June 1997
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 108 (6) , 923-927
- https://doi.org/10.1111/1523-1747.ep12294634
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Mouse Pale Ear (ep) is Homologous to Human Hermansky-Pudlak Syndrome and Contains a Rare 'AT-AC' IntronHuman Molecular Genetics, 1997
- U1-Mediated Exon Definition Interactions Between AT-AC and GT-AG IntronsScience, 1996
- Positional cloning of a gene for Hermansky–Pudlak syndrome, a disorder of cytoplasmic organellesNature Genetics, 1996
- Requirement of U12 snRNA for in Vivo Splicing of a Minor Class of Eukaryotic Nuclear Pre-mRNA IntronsScience, 1996
- A Novel Spliceosome Containing U11, U12, and U5 snRNPs Excises a Minor Class (AT–AC) Intron In VitroCell, 1996
- Linkage disequilibrium mapping of the gene for Hermansky-Pudlak syndrome to chromosome 10q23. 1-q23.3Human Molecular Genetics, 1995
- Conserved Sequences in a Class of Rare Eukaryotic Nuclear Introns with Non-consensus Splice SitesJournal of Molecular Biology, 1994
- Hermansky-Pudlak Syndrome in a Swiss PopulationDermatology, 1993
- A reappraisal of non-consensus mRNA splice sitesNucleic Acids Research, 1991
- The Melanin Pigmentary Disorder in a Family with Hermansky-Pudlak SyndromeJournal of Investigative Dermatology, 1982