Expression and Cloning of the Human X-Linked Hypophosphatemia Gene cDNA

X-linked hypophosphatemia (XLH), which is a heritable metabolic bone disease characterized biochemically by selective renal phosphate (Pi) wasting, is associated with mutations in the PEX (Phosphate-regulating gene with homologies toEndopeptidases on theX-chromosome) gene. To further explore the phy...

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Veröffentlicht in:	Biochemical and biophysical research communications 1997-02, Vol.231 (3), p.635-639
Hauptverfasser:	Grieff, Marvin, Mumm, Steven, Waeltz, Paul, Mazzarella, Richard, Whyte, Michael P, Thakker, Rajesh V, Schlessinger, David
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Sequence Base Sequence Cloning, Molecular DNA, Complementary - genetics Gene Expression Humans Hypophosphatemia - genetics Introns Molecular Sequence Data PHEX Phosphate Regulating Neutral Endopeptidase Point Mutation Proteins - genetics RNA, Messenger - genetics Species Specificity X Chromosome
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