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Characterization of two iPSC lines from patients with maternally inherited leigh (MILS) and neuropathy, ataxia, and retinitis pigmentosa (NARP) syndrome carrying the MT-ATP6 m.8993 T>G mutation at different degrees of heteroplasmy

Stem Cell Research
2024-09 | Journal article
Part of ISSN: 1873-5061
Contributors: Anna Maria Haschke; Sebastian Diecke; Markus Schuelke
Source: Self-asserted source
Anna Maria Haschke

Establishment and Characterization of hTERT Immortalized Hutchinson–Gilford Progeria Fibroblast Cell Lines

Cells
2022-09-06 | Journal article
Part of ISSN: 2073-4409
Contributors: Anna Maria Haschke
Source: Self-asserted source
Anna Maria Haschke
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