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A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy von Al-Hassnan, Zuhair N, Shinwari, Zarghuna Ma, Wakil, Salma M, Tulbah, Sahar, Mohammed, Shamayel, Rahbeeni, Zuhair, Alghamdi, Mohammed, Rababh, Monther, Colak, Dilek, Kaya, Namik, Al-Fayyadh, Majid, Alburaiki, Jehad

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Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemia von Kaya, Namik, Colak, Dilek, Al-Bakheet, Albandary, Al-Younes, Banan, Tulbah, Sahar, Daghestani, Maha, Al-Mutairi, Fuad, Al-Amoudi, Mohammed, Al-Odaib, Ali, Al-Aqeel, Aida I.

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Additional file 1: Table S1. of A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy von Al-Hassnan, Zuhair, Zarghuna Shinwari, Wakil, Salma, Tulbah, Sahar, Shamayel Mohammed, Rahbeeni, Zuhair, Alghamdi, Mohammed, Rababh, Monther, Colak, Dilek, Kaya, Namik, Al-Fayyadh, Majid, Alburaiki, Jehad

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