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Species Resource Title
Human and Animal Cells Tissue-specific distribution of an alternatively spliced COL4A5 isoform and non-random X chromosome inactivation reflect phenotypic variation in heterozygous X-linked Alport syndrome.
Human and Animal Cells ΔRad51C-DT40 (RCB1623) Mutation of the RAD51C gene in a Fanconi anemia-like disorder.