A novel deletion mutation in the ALOX12B gene in a Kurdish family with autosomal recessive congenital ichthyosis

J Eur Acad Dermatol Venereol. 2016 Nov;30(11):e144-e145. doi: 10.1111/jdv.13457. Epub 2015 Nov 16.

I B Lolas^{1

2}, M Sommerlund³, H Okkels⁴, M Ramsing⁵, M B Petersen^{6

7}

¹ Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark. i.lolas@rn.dk.
² Section of Molecular Diagnostics, Department of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark. i.lolas@rn.dk.
³ Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.
⁴ Section of Molecular Diagnostics, Department of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark.
⁵ Institute of Pathology, Aarhus University Hospital, Aarhus, Denmark.
⁶ Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.
⁷ Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

No abstract available

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