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Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern.
Clin Exp Nephrol. 2017 Aug;21(4):677-684. doi: 10.1007/s10157-016-1331-3. Epub 2016 Aug 29.
Clin Exp Nephrol. 2017.
PMID: 27573339
[Congenital ciliary dysfunction in children].
Korppi M, Dunder T, Remes S, Sjöström PM, Holm T, Vähäsarja V, Jartti T, Pääkkö P, Kajosaari M.
Korppi M, et al. Among authors: sjostrom pm.
Duodecim. 2011;127(21):2294-302.
Duodecim. 2011.
PMID: 22204144
Review.
Finnish.
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