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Article

The hereditary stomatocytoses and allied disorders: congenital disorders of erythrocyte membrane permeability to Na and K

1 Dec 1999

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10895260
DOI: 10.1053/beha.1999.0049

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Related research

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The hereditary stomatocytoses and allied disorders: congenital disorders of erythrocyte membrane permeability to Na and KPMID 10895260Read ↗

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The cation‐leaky hereditary stomatocytosis syndromes: A tale of six proteinsSemantic proximity Read ↗

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Stomatocytosis of Standard Schnauzers is not associated with stomatin deficiency.Semantic proximity Read ↗

Cation-leak stomatocytosis in standard schnauzers does not cosegregate with coding mutations in the RhAG, SLC4A1, or GLUT1 genes associated with human disease.Semantic proximity Read ↗

Isolation of cDNA coding for an ubiquitous membrane protein deficient in high Na+, low K+ stomatocytic erythrocytes.Semantic proximity Read ↗

Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S.Semantic proximity Read ↗

The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein.Semantic proximity Read ↗

Dehydrated hereditary stomatocytosis: Prenatal management of ascites and pleural effusions.Semantic proximity Read ↗

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