Copy number loss in SFMBT1 is...

Neurology: Genetics 2018 / 12 Vol. 4; Iss. 6

Copy number loss in SFMBT1 is common among Finnish and Norwegian patients with iNPH

Korhonen, Ville E., Helisalmi, Seppo, Jokinen, Aleksi, Jokinen, Ilari, Lehtola, Juha-Matti, Oinas, Minna, Lönnrot, Kimmo, Avellan, Cecilia, Kotkansalo, Anna, Frantzen, Janek, Rinne, Jaakko, Ronkainen,
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Volume:
4
Language:
english
Journal:
Neurology Genetics
DOI:
10.1212/NXG.0000000000000291
Date:
December, 2018
File:
PDF, 346 KB
english, 2018
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