Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome

D. J. Ralser; S. Kumar; O. Borisov; O. Sarig; G. Richard; S. Wolf; P. M. Krawitz; E. Sprecher; M. Kreiß; R. C. Betz

doi:10.1111/bjd.19123

Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome

D. J. Ralser, S. Kumar, O. Borisov, O. Sarig, G. Richard, S. Wolf, P. M. Krawitz, E. Sprecher, M. Kreiß, R. C. Betz^*

^*Corresponding author for this work

Dermatology

Research output: Contribution to journal › Letter › peer-review

3 Scopus citations

Original language	English
Pages (from-to)	756-757
Number of pages	2
Journal	British Journal of Dermatology
Volume	183
Issue number	4
DOIs	https://doi.org/10.1111/bjd.19123
State	Published - 1 Oct 2020

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10.1111/bjd.19123

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author = "Ralser, {D. J.} and S. Kumar and O. Borisov and O. Sarig and G. Richard and S. Wolf and Krawitz, {P. M.} and E. Sprecher and M. Krei{\ss} and Betz, {R. C.}",

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AU - Richard, G.

AU - Wolf, S.

AU - Krawitz, P. M.

AU - Sprecher, E.

AU - Kreiß, M.

AU - Betz, R. C.

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Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome

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