Associated Papers
Novel Intragenic and Genomic Variants Highlight the Phenotypic Variability in HCCS-Related Disease.
Reis LM et al.
Genes, 2024
Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome.
Dambietz CA et al.
Frontiers in Genetics, 2024
39233738 (PubMed )
Supplement: Table1.XLSX › Tabelle1
Genetic Profile of Left Ventricular Noncompaction Cardiomyopathy in Children-A Single Reference Center Experience.
Piekutowska-Abramczuk D et al.
Genes, 2022
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