Missense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma Multiplex - Concepedia

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Missense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma Multiplex

DOI Full Paper Access

167

Citations

13

References

1997

Year

Frances J.D. Smith, Laura D. Corden, E.L. Rugg, R. Ratnavel, Irene M. Leigh, Celia Moss, Michael J. Tidman, Daniel Hohl, Marcel Huber, L. Kunkeler,

Journal of Investigative Dermatology

Missense MutationsGeneticsPathologyKeratin 17MedicineMolecular Medicine

References

	Year	Citations

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