X-linked Alport syndrome in Hellenic families: Phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5
P. Demosthenous, K. Voskarides, K. Stylianou, M. Hadjigavriel, M. Arsali, C. Patsias, E. Georgaki, P. Zirogiannis, C. Stavrou, E. Daphnis, A. Pierides, C. Deltas
Research output: Contribution to journal › Article › peer-review
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