R162W Mutation of Keratin 9 in a Family with Autosomal Dominant Palmoplantar Keratoderma with Unique Histologic Features - Concepedia

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R162W Mutation of Keratin 9 in a Family with Autosomal Dominant Palmoplantar Keratoderma with Unique Histologic Features

DOI Full Paper Access

14

Citations

28

References

1999

Year

Nobuyasu Mayuzumi, Takako Shigihara, Shigaku Ikeda, Hideoki Ogawa

Journal of Investigative Dermatology Symposium Proceedings

Skin DevelopmentUnique Histologic FeaturesGeneticsPathologyMolecular GeneticsR162w MutationDermatologyDermatopathologyMedicineKeratin 9Skin Cancer

References

	Year	Citations

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