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pro vyhledávání: '"Ioanelli Petrou"'
Autor:
Konstantinos Voskarides, Gregory Papagregoriou, Despina Hadjipanagi, Ioanelli Petrou, Isavella Savva, Avraam Elia, Yiannis Athanasiou, Androulla Pastelli, Maria Kkolou, Michalis Hadjigavriel, Christoforos Stavrou, Alkis Pierides, Constantinos Deltas
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-8 (2018)
Abstract Background About 40–50% of patients with familial microscopic hematuria (FMH) caused by thin basement membrane nephropathy (TBMN) inherit heterozygous mutations in collagen IV genes (COL4A3, COL4A4). On long follow-up, the full phenotypic
Externí odkaz:
https://doaj.org/article/60ea5110388c4002b20d58a5ee9ce72a
Autor:
Voskarides, Konstantinos, Papagregoriou, Gregory, Hadjipanagi, Despina, Ioanelli Petrou, Savva, Isavella, Avraam Elia, Yiannis Athanasiou, Androulla Pastelli, Kkolou, Maria, Hadjigavriel, Michalis, Stavrou, Christoforos, Pierides, Alkis, Constantinos Deltas
WES statistics. Number of genetic variants called after the WES analysis. (DOCX 15 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5180278783d94eeaaf7f18f08eb79a8e