Frida Jonsson

Medical and Clinical Genetics

Publications

Author

Title

Year sorteringsordning

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Frida, Jonsson

Underlying genetic mechanisms of hereditary dystrophies in retina and cornea

2017

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Golovleva, Irina
Jonsson, Frida
Burstedt, Marie

Heterogeneity and complexity of EYS mutations in autosomal recessive retinitis pigmentosa in northern Sweden
Investigative Ophthalmology and Visual Science, 57(12)

2016

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Jonsson, Frida
Byström, Berit
Davidson, Alice E.; et al.

Mutations in Collagen, Type XVII, Alpha 1 (COL17A1) Cause Epithelial Recurrent Erosion Dystrophy (ERED)
Human Mutation, 36(4): 463-473

2015

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Jonsson, Frida
Burstedt, Marie S
Sandgren, Ola; et al.

Genetic heterogeneity and clinical outcome in a Swedish family with retinal degeneration caused by mutations in CRB1 and ABCA4 genes
Retinal Degenerative Diseases: 177-183

2014

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Jonsson, Frida
Burstedt, Marie S
Sandgren, Ola; et al.

Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family
European Journal of Human Genetics, 21(11): 1266-1271

2013

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Burstedt, Marie
Jonsson, Frida
Köhn, Linda; et al.

Genotype-phenotype correlations in Bothnia dystrophy caused by RLBP1 gene sequence variations
Acta Ophthalmologica, 91(5): 437-444

2013

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