Genomic organization and alternative transcripts of the human PQBP-1 gene
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference22 articles.
1. Trinucleotide repeat expansion and human disease;Ashley;Annu. Rev. Genet.,1995
2. Nucleotide sequence of XLPOU3 cDNA, a member of the POU-domain gene family expressed in Xenopus laevis embryos;Baltzinger;Nucleic Acids Res.,1992
3. Transcription of XLPOU3, a brain specific gene, during Xenopus laevis early embryogenesis;Baltzinger;Mech. Dev.,1996
4. Sry requires a CAG repeat domain for male sex determination in Mus musculus;Bowles;Nat. Genet.,1999
5. Organization and expression of eucaryotic split genes coding for proteins;Breathnach;Annu. Rev. Biochem.,1981
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