Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders - Concepedia

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Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

151

Citations

21

References

1997

Year

Herma Portsteffen, Andreas Beyer, E. Becker, Cornelia Epplen, André Pawlak, Wolf‐H. Kunau, Gabriele Dodt

Nature Genetics

Complementation Group 1Peroxisome Biogenesis DisordersMendelian DisorderGenetic DisorderGeneticsGenetic MechanismMolecular GeneticsDisease Gene IdentificationHuman Pex1Gene ExpressionMedicineCell BiologyCell Development

References

	Year	Citations

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