A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome

N. Kaçar; N. Semerci; Ş Ergin; M. Pascucci; G. Zambruno; D. Castiglia

doi:10.1111/j.1365-2133.2008.08553.x

A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome

N. Kaçar, N. Semerci, Ş Ergin, M. Pascucci, G. Zambruno, D. Castiglia

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	1375-1377
Number of pages	3
Journal	British Journal of Dermatology
Volume	158
Issue number	6
DOIs	https://doi.org/10.1111/j.1365-2133.2008.08553.x
Publication status	Published - Jun 2008

Keywords

KIND1
Kindler syndrome
Mutation database
Poikiloderma

ASJC Scopus subject areas

Dermatology

Access to Document

10.1111/j.1365-2133.2008.08553.x

Cite this

Kaçar, N., Semerci, N., Ergin, Ş., Pascucci, M., Zambruno, G., & Castiglia, D. (2008). A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome. British Journal of Dermatology, 158(6), 1375-1377. https://doi.org/10.1111/j.1365-2133.2008.08553.x

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