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Browsing by Author Krick, Stefanie

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Issue DateTitleAuthor(s)Type
2-May-2011COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessHeeringa, Saskia F.; Chernin, Gil; Chaki, Moumita; Zhou, Weibin; Sloan, Alexis J.; Ji, Ziming; Xie, Letian X.; Salviati, Leonardo; Hurd, Toby W.; Vega-Warner, Virginia; Killen, Paul D.; Raphael, Yehoash; Ashraf, Shazia; Ovunc, Bugsu; Schoeb, Dominik S.; McLaughlin, Heather M.; Airik, Rannar; Vlangos, Christopher N.; Gbadegesin, Rasheed; Hinkes, Bernward; Saisawat, Pawaree; Trevisson, Eva; Doimo, Mara; Casarin, Alberto; Pertegato, Vanessa; Giorgi, Gianpietro; Prokisch, Holger; Rötig, Agnès; Nürnberg, Gudrun; Becker, Christian; Wang, Su; Ozaltin, Fatih; Topaloglu, Rezan; Bakkaloglu, Aysin; Bakkaloglu, Sevcan A.; Müller, Dominik; Beissert, Antje; Mir, Sevgi; Berdeli, Afig; ϖzen, Seza; Zenker, Martin; Matejas, Verena; Santos-Ocaña, Carlos; Navas, Plácido; Kusakabe, Takehiro; Kispert, Andreas; Akman, Sema; Soliman, Neveen A.; Krick, Stefanie; Mundel, Peter; Reiser, Jochen; Nürnberg, Peter; Clarke, Catherine F.; Wiggins, Roger C.; Faul, Christian; Hildebrandt, FriedhelmArtículo

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