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The molecular and genetic base of congenital transport defects.

作者信息

Desjeux J F

机构信息

Conservatoire National des Arts et Métiers Paris, France.

出版信息

Gut. 2000 May;46(5):585-7. doi: 10.1136/gut.46.5.585.

Abstract
摘要

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Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.
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Genetic disorders of membrane transport. IV. Wilson's disease and Menkes disease.
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Genetic homogeneity of lysinuric protein intolerance.
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I. Glucose galactose malabsorption.
Am J Physiol. 1998 Nov;275(5):G879-82. doi: 10.1152/ajpgi.1998.275.5.G879.
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