Tissue differences in the expression of mutations and polymorphisms in the GRHPR gene and implications for diagnosis of primary hyperoxaluria type 2

Tissue differences in the expression of mutations and polymorphisms in the GRHPR gene and implications for diagnosis of primary hyperoxaluria type 2

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Veröffentlicht in:Clinical chemistry (Baltimore, Md.) Md.), 2005-12, Vol.51 (12), p.2423-2425
Hauptverfasser: Bhat, Swati, Williams, Emma L, Rumsby, Gill
Format: Artikel
Sprache:eng
Schlagworte:
Alcohol Oxidoreductases - genetics
Base Sequence
DNA, Complementary - genetics
Gene Expression Regulation - genetics
Humans
Hyperoxaluria, Primary - diagnosis
Hyperoxaluria, Primary - genetics
Internet
Leukocytes - metabolism
Liver - metabolism
Molecular Sequence Data
Mutation - genetics
Organ Specificity
Polymorphism, Genetic - genetics
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container_issue 12
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container_title Clinical chemistry (Baltimore, Md.)
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creator Bhat, Swati
Williams, Emma L
Rumsby, Gill
description
doi_str_mv 10.1373/clinchem.2005.058305
format Article
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current)
subjects Alcohol Oxidoreductases - genetics
Base Sequence
DNA, Complementary - genetics
Gene Expression Regulation - genetics
Humans
Hyperoxaluria, Primary - diagnosis
Hyperoxaluria, Primary - genetics
Internet
Leukocytes - metabolism
Liver - metabolism
Molecular Sequence Data
Mutation - genetics
Organ Specificity
Polymorphism, Genetic - genetics
title Tissue differences in the expression of mutations and polymorphisms in the GRHPR gene and implications for diagnosis of primary hyperoxaluria type 2
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