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A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome. [electronic resource] by
- Bredrup, Cecilie
- Stokowy, Tomasz
- McGaughran, Julie
- Lee, Samuel
- Sapkota, Dipak
- Cristea, Ileana
- Xu, Linda
- Tveit, Kåre Steinar
- Høvding, Gunnar
- Steen, Vidar Martin
- Rødahl, Eyvind
- Bruland, Ove
- Houge, Gunnar
Producer: 20200615
In:
European journal of human genetics : EJHG vol. 27
Availability: No items available.
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13.
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Nordic research in ophthalmology. [electronic resource] by
- Heijl, Anders
- Algvere, Peep V
- Alm, Albert
- Andersen, Nis
- Bauer, Birgitta
- Carlsson, Jan-Olof
- Ehinger, Berndt
- Eide, Nils
- Fledelius, Hans
- Foerster, Michael
- Hjortdal, Jesper
- Holmström, Gerd
- Høvding, Gunnar
- Kivelä, Tero
- la Cour, Morten
- Lindblom, Bertil
- Møller-Pedersen, Torben
- Nikoskelainen, Eeva
- Prause, Jan Ulrik
- Riise, Ruth
- Rosenberg, Thomas
- Seregard, Stefan
- Stefánsson, Einar
- Tarkkanen, Ahti
- Tervo, Timo
- Tornqvist, Kristina
- Zetterström, Charlotta
Producer: 20050711
In:
Acta ophthalmologica Scandinavica vol. 83
Availability: No items available.
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