Associated Papers
Clinical Features and Novel Pathogenic Variants of Chinese Patients With McLeod Syndrome and Chorea-Acanthocytosis.
Yu H et al.
Molecular Genetics & Genomic Medicine, 2024
A case of McLeod syndrome caused by a nonsense variation c.942G>A in the XK gene: A case report.
Ying Y et al.
Frontiers in Genetics, 2023
Three new XK alleles; two associated with a McLeod RBC phenotype.
Floch A et al.
Transfusion, 2021
McLeod neuroacanthocytosis: genotype and phenotype.
Danek A et al.
Annals of Neurology, 2001
A spontaneous novel XK gene mutation in a patient with McLeod syndrome.
Supple SG et al.
British Journal of Haematology, 2001
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