Resultats de la cerca - Imen Rejeb
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First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations per Imen Rejeb, Houweyda Jilani, Yasmina Elaribi, Syrine Hizem, Lamia Hila, Julia Lauer Zillahrdt, Jamel Chelly, Lamia Benjemaa
Publicat 2017Signatura: Carregant…Connect to this object online.
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2
New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 gene per Imen Rejeb, Mouna Jerbi, Houweyda Jilani, Hanène Gaied, Yasmina Elaribi, Syrine Hizem, Raja Aoudia, Hafedh Hedri, Chiraz Zaied, Salwa Abid, Hassen Bacha, Taieb BenAbdallah, Lamia BenJemaa, Rim Goucha
Publicat 2021Signatura: Carregant…Connect to this object online.
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