Risultati della ricerca - Asadollahi, Mostafa
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Whole-Exome Sequencing Identified a Novel Variant (C.405_422+39del) in DSP Gene in an Iranian Pedigree with Familial Dilated Cardiomyopathy di Eshaghkhani, Yeganeh, Mohamadifar, Arezoo, Asadollahi, Mostafa, Taghizadeh, Mahdieh, Karamzade, Arezou, Saberi, Mohammad, Nourmohammadi, Parisa, Golchehre, Zahra, Amin, Ahmad, Keramatipour, Mohammad
Pubblicazione 2021testo -
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Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families di AKBAROGHLI, Susan, KOOSHAVAR, Daniz, GOLCHEHRE, Zahra, KARAMZADE, Arezou, SABERI, Mohammad, ALAEI, Mohammad Reza, ABBASI SADEGH, Masoud, ASADOLLAHI, Mostafa, KERAMATIPOUR, Mohammad
Pubblicazione 2022testo -
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Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome di Latour, Brooke L., Van De Weghe, Julie C., Rusterholz, Tamara D.S., Letteboer, Stef J.F., Gomez, Arianna, Shaheen, Ranad, Gesemann, Matthias, Karamzade, Arezou, Asadollahi, Mostafa, Barroso-Gil, Miguel, Chitre, Manali, Grout, Megan E., van Reeuwijk, Jeroen, van Beersum, Sylvia E.C., Miller, Caitlin V., Dempsey, Jennifer C., Morsy, Heba, Bamshad, Michael J., Nickerson, Deborah A., Neuhauss, Stephan C.F., Boldt, Karsten, Ueffing, Marius, Keramatipour, Mohammad, Sayer, John A., Alkuraya, Fowzan S., Bachmann-Gagescu, Ruxandra, Roepman, Ronald, Doherty, Dan
Pubblicazione 2020testo