Genomic Organization and Complete Nucleotide Sequence of the TMEM1 Gene on Human Chromosome 21q22.3

This publication has 14 references indexed in Scilit:

• One-megabase sequence analysis of the human immunoglobulin lambda gene locus.
  Genome Research, 1997
• Localization of 16 Exons to a 450-kb Region Involved in the Autoimmune Polyglandular Disease Type I (APECED) on Human Chromosome 21q22.3
  DNA Research, 1997
• Isolation of cDNA for a Novel Human Protein KNP-I That Is Homologous to theE. coliSCRP-27A Protein from the Autoimmune Polyglandular Disease Type I (APECED) Region of Chromosome 21q22.3
  Biochemical and Biophysical Research Communications, 1996
• A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3
  Human Molecular Genetics, 1996
• Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1)
  Science, 1996
• Autosomal Recessive Non-Syndromic Deafness Locus (DFNB8) Maps on Chromosome 21Q22 in a Large Consanguineous Kindred from Pakistan
  Human Molecular Genetics, 1996
• Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3
  Human Molecular Genetics, 1995
• A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3
  Nature Genetics, 1994
• An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21
  Nature Genetics, 1994
• Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping
  Human Molecular Genetics, 1993