PEX7 Gene Structure, Alternative Transcripts, and Evidence for a Founder Haplotype for the Frequent RCDP Allele, L292ter

This publication has 49 references indexed in Scilit:

• X-Linked Late-Onset Sensorineural Deafness Caused by a Deletion Involving OA1 and a Novel Gene Containing WD-40 Repeats
  American Journal of Human Genetics, 1999
• Identification of PAHX, a Refsum disease gene
  Nature Genetics, 1997
• Point Mutations and an Intragenic Deletion in LIS1, the Lissencephaly Causative Gene in Isolated Lissencephaly Sequence and Miller-Dieker Syndrome
  Human Molecular Genetics, 1997
• A unified nomenclature for peroxisome biogenesis factors.
  The Journal of cell biology, 1996
• Detection of p53 Mutations by Single-strand Conformation Polymorphisms (SSCP) Gel Electrophoresis
  Diagnostic Molecular Pathology, 1995
• The ancient regulatory-protein family of WD-repeat proteins
  Nature, 1994
• BIOCHEMISTRY OF PEROXISOMES
  Annual Review of Biochemistry, 1992
• Control of the peroxisomal β-oxidation pathway by a novel family of nuclear hormone receptors
  Published by Elsevier ,1992
• Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting
  Biochemical and Biophysical Research Communications, 1991
• Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators
  Nature, 1990