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Linda Köhn

Kontaktinformation
Befattning:	Forskningsingenjör, förste
Verksam vid:	Medicinsk biovetenskap
Avdelning:	Patologi
Adress:	Umeå universitet SE-901 85 Umeå Sverige
Besöksadress:	By 6M, vån 3, Sjukhusområdet
Tel:	+46 90 785 28 73
Fax:	+46 90 13 07 60
E-postadress:	linda.kohn@medbio.umu.se E-post
Webbsida:	http://www.medbio.umu.se/om-institutionen/personal/kohn-linda/ Webbsida

Publikationer

Författare	Titel	År	Fulltext
Reinis, Ainars Golovleva, Irina Köhn, Linda; et al.	Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation Acta Ophthalmologica, 91(3): 259-266	2013	-
Golovleva, Irina Köhn, Linda Burstedt, Marie; et al.	Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern sweden. Advances in Experimental Medicine and Biology, 664: 255-262	2010	-
Köhn, Linda Kohl, Susanne Bowne, Sara J; et al.	PITPNM3 is an uncommon cause of cone and cone-rod dystrophies. Ophthalmic Genetics, 31(3): 139-140	2010	-
Köhn, Linda Bowne, Sara J S Sullivan, Lori; et al.	Breakpoint characterization of a novel approximately 59 kb genomic deletion on 19q13.42 in autosomal-dominant retinitis pigmentosa with incomplete penetrance. European Journal of Human Genetics, 17(5): 651-655	2009	-
Köhn, Linda Bowne, Sara J Daiger, Stephen P; et al.	Breakpoint characterization of a novel ~59 kb genomic deletion on 19q13.42 in autosomal dominant retinitis pigmentosa with reduced penetrance European Journal of Human Genetics, 17(5): 651-655	2009	-
Köhn, Linda Burstedt, Marie SI Jonsson, Frida; et al.	Carrier of R14W in carbonic anhydrase IV presents Bothnia dystrophy phenotype caused by two allelic mutations in RLBP1 Investigative Ophthalmology and Visual Science, 49(7): 3172-3177	2008	-
Köhn, Linda Kadzhaev, Konstantin Burstedt, Marie S I; et al.	Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families. Recent Advances in Retinal Degeneration: 229-234	2008	-
Köhn, Linda Kadzhaev, Konstantin Burstedt, Marie SI; et al.	Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families European Journal of Human Genetics, 15(6): 664-671	2007	-

Sidansvarig: Åsa Lundsten
2010-11-02