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Refined by: Subject: Mutation remove
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Diminished protein‐bound ω‐hydroxylated ceramides in the skin of patients with ichthyosis with 12R‐lipoxygenase (LOX) or eLOX‐3 deficiency

Dick, A. ; Tantcheva‐Poór, I. ; Oji, V. ; Giehl, K. A. ; Fischer, J. ; Krieg, P. ; Schneider, H. ; Rauh, M.

British Journal of Dermatology, October 2017, Vol.177(4), pp.e119-e121 [Peer Reviewed Journal]

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Pili annulati: refinement of the locus on chromosome 12q24.33 to a 2·9‐Mb interval and candidate gene analysis

Giehl, K. A. ; Rogers, M. A. ; Radivojkov, M. ; Tosti, A. ; De Berker, D. A. R. ; Weinlich, G. ; Schmuth, M. ; Ruzicka, T. ; Eckstein, G. N.

British Journal of Dermatology, March 2009, Vol.160(3), pp.527-533 [Peer Reviewed Journal]

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Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study

Vural, S. ; Gündoğdu, M. ; Gökpınar İli, E. ; Durmaz, C. D. ; Vural, A. ; Steinmüller‐Magin, L. ; Kleinhempel, A. ; Holdt, L. M. ; Ruzicka, T. ; Giehl, K. A. ; Ruhi, H. I. ; Boyvat, A.

British Journal of Dermatology, June 2019, Vol.180(6), pp.1459-1467 [Peer Reviewed Journal]

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Pyrin mutations in complex hidradenitis suppurativa

Vural, S. ; Gündoğdu, M. ; Gökpınar İli, E. ; Durmaz, C. D. ; Vural, A. ; Steinmüller‐Magin, L. ; Kleinhempel, A. ; Holdt, L. M. ; Ruzicka, T. ; Giehl, K. A. ; Ruhi, H. I. ; Boyvat, A.

British Journal of Dermatology, June 2019, Vol.180(6), pp.e244-e244 [Peer Reviewed Journal]

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Hair interior defect in AKR/J mice

Giehl, K. A. ; Potter, C. S. ; Wu, B. ; Silva, K. A. ; Rowe, L. B. ; Awgulewitsch, A. ; Sundberg, J. P.

Clinical and Experimental Dermatology, June 2009, Vol.34(4), pp.509-517 [Peer Reviewed Journal]

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