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Journal article

Expression and cloning of the human X-linked hypophosphatemia gene cDNA.

Abstract:

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 to Endopeptidases on the X-chromosome) gene. To further explore the physiologic role of PEX and define its effect in XLH we have determined the expression and tissue distribution. Northern analysis found abundant PEX mRNA in a restricted pattern, predominantly in ad...

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Publication status:
Published

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Publisher copy:
10.1006/bbrc.1997.6153

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Journal:
Biochemical and biophysical research communications
Volume:
231
Issue:
3
Pages:
635-639
Publication date:
1997-02-05
DOI:
EISSN:
1090-2104
ISSN:
0006-291X
URN:
uuid:606b4cd9-61b6-4ec6-a725-9292e134b556
Source identifiers:
11197
Local pid:
pubs:11197

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