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

4 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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title = "Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome",

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 - Borisov, O.

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AU - Richard, G.

AU - Wolf, S.

AU - Krawitz, P. M.

AU - Sprecher, E.

AU - Kreiß, M.

AU - Betz, R. C.

PY - 2020/10/1

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

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