Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease
SourceOrphanet Journal of Rare Diseases, 15, 1, (2020), article 36
Article / Letter to editor
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Orphanet Journal of Rare Diseases
SubjectAll institutes and research themes of the Radboud University Medical Center; Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences
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