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A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging
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Homozygous human TAP peptide transporter mutation in HLA class I deficiency

H de la Salle1, D Hanau, D Fricker

  • 1Laboratoire d'Histocompatibilité, Centre Régional de Transfusion Sanguine, Strasbourg, France.

Science (New York, N.Y.)
|July 8, 1994
PubMed

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