X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males

Autor:	Jp, Jais, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Ko, Netzer, Flinter F, Pirson Y, Verellen C, Wieslander J, Persson U, Tryggvason K, Martin P, Jm, Hertz, Schröder C, Sanak M, Marie-Claire Gubler
Zdroj:	CIÊNCIAVITAE Europe PubMed Central
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1e748613fe947a7c9b656e6a9074ec6d http://europepmc.org/abstract/med/10752524 Zobrazit plný text záznamu