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Cell Line | Cell Line Alias | Cell Type | Disease | Genetic Alteration/Mutation | Sex | Age at Collection | Ethnicity | Genetically Related Cell Lines | dbGaP Data |
|---|---|---|---|---|---|---|---|---|---|
FX13-2 | Human iPS | Fragile X syndrome | Male | 8 Years | No | No | |||
C603-4 | Human iPS | None reported | Male | 36 Years | No | No | |||
Human iPS | Charcot-Marie-Tooth disease type 2A | S249T mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene | Male | No | No | ||||
Human iPS | Charcot-Marie-Tooth disease type 2A | S249T mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene | Male | No | No | ||||
Human iPS | Charcot-Marie-Tooth disease type 2A | S249T mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene | Male | No | No | ||||
Human iPS | Charcot-Marie-Tooth disease type 2A | H361y mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene | Male | Yes | No | ||||
Human iPS | Charcot-Marie-Tooth disease type 2A | H361y mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene | Male | Yes | No | ||||
Human iPS | Charcot-Marie-Tooth disease type 2A | H361y mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene | Male | Yes | No | ||||
Human iPS | None reported | Male | Yes | No | |||||
Human iPS | None reported | Male | Yes | No |