Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease - Concepedia

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Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease

DOI Full Paper Access

67

Citations

26

References

1998

Year

Anneke M. Sijbers, Pieter C. van Voorst Vader, J. W. Snoek, Anja Raams, Nicolaas G.J. Jaspers, Wim J. Kleijer

Journal of Investigative Dermatology

Xpf GeneNeurodegenerative DiseasesXeroderma PigmentosumMendelian DisorderGenetic DisorderGeneticsPathologyDegenerative DiseaseLate-onset Neurologic DiseaseNeurologyDisease Gene IdentificationNeuropathologyMedicine

References

	Year	Citations

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