Associated Papers
A new variant in the ZCCHC8 gene: diverse clinical phenotypes and expression in the lung.
Groen K et al.
Erj Open Research, 2024
38375433 (PubMed )
Supplement: 00487-2023.SUPPLEMENT.pdf
Genetic Variant Overlap Analysis Identifies Established and Putative Genes Involved in Pulmonary Fibrosis.
Groen K et al.
International Journal of Molecular Sciences, 2023
36769106 (PubMed )
Supplement: ijms-24-02790-s001.zip › ijms-2132947-supplementary.pdf
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.
Zhou Y et al.
Bmc Medical Genetics, 2020
32682410 (PubMed )
Supplement: 12881_2020_1087_MOESM1_ESM.xlsx › HL2
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