Functional expression and cellular distribution of diastrophic dysplasia sulfate transporter ( DTDST ) gene mutations in HEK cells

Author： Karniski Lawrence P.

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.13, Iss.19, 2004-10, pp. : 2165-2171

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Mutations in the diastrophic dysplasia sulfate transporter ( DTDST ) gene: correlation between sulfate transport activity and chondrodysplasia phenotype

By Karniski L.P.

Human Molecular Genetics, Vol. 10, Iss. 14, 2001-07 ,pp. : 1485-1490

Oxford University Press

Access to resources Recommend Favorite

A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype

By Forlino Antonella

Human Molecular Genetics, Vol. 14, Iss. 6, 2005-03 ,pp. : 859-871

Oxford University Press

Access to resources Recommend Favorite

Functional analysis of novel mutations in y + LAT-1 amino acid transporter gene causing lysinuric protein intolerance (LPI)

By Mykkänen Juha

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 431-438

Oxford University Press

Access to resources Recommend Favorite

Functional annotation of mouse mutations in embryonic stem cells by use of expression profiling

By Symula Derek

Mammalian Genome, Vol. 15, Iss. 1, 2004-01 ,pp. : 1-13

Springer Publishing Company

Access to resources Recommend Favorite

Mutations of OCTN2 , an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency

By Ganapathy V.

Human Molecular Genetics, Vol. 8, Iss. 4, 1999-04 ,pp. : 655-660

Oxford University Press

Access to resources Recommend Favorite