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A Homozygous Missense Mutation in the Ciliary Gene TTC21B Causes Familial FSGS
Cong, E. H., Bizet, A. A., Boyer, O., Woerner, S., Gribouval, O., Filhol, E., Arrondel, C., Thomas, S., Silbermann, F., Canaud, G., Hachicha, J., Ben Dhia, N., Peraldi, M.-N., Harzallah, K., Iftene, DVolume:
25
Language:
english
Journal:
Journal of the American Society of Nephrology
DOI:
10.1681/ASN.2013101126
Date:
November, 2014
File:
PDF, 1.94 MB
english, 2014