TY - DATA T1 - Additional file 1: Table S1. of A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy PY - 2016/01/14 AU - Zuhair Al-Hassnan AU - Zarghuna Shinwari AU - Salma Wakil AU - Sahar Tulbah AU - Shamayel Mohammed AU - Zuhair Rahbeeni AU - Mohammed Alghamdi AU - Monther Rababh AU - Dilek Colak AU - Namik Kaya AU - Majid Al-Fayyadh AU - Jehad Alburaiki UR - https://springernature.figshare.com/articles/journal_contribution/Additional_file_1_Table_S1_of_A_substitution_mutation_in_cardiac_ubiquitin_ligase_FBXO32_is_associated_with_an_autosomal_recessive_form_of_dilated_cardiomyopathy/4349804 DO - 10.6084/m9.figshare.c.3606797_D1.v1 L4 - https://ndownloader.figshare.com/files/7075850 KW - Cardiomyopathy KW - FBXO32 KW - Ubiquitin proteasome system N2 - Forty-eight OMIM genes implicated in dilated and hypertrophic familial cardiomyopathy that were screened for all the homozygous variants detected by whole exome sequencing. All of the identified 62 variants have been previously reported in the dbSNP and/or 1000 Genomes databases as polymorphisms, except for two novel variants in TNN and SGCD genes, which were found to be intronic. (DOCX 17 kb) ER -