10.6084/m9.figshare.c.3606797_D1.v1
Zuhair Al-Hassnan
Zuhair
Al-Hassnan
Zarghuna Shinwari
Zarghuna
Shinwari
Salma Wakil
Salma
Wakil
Sahar Tulbah
Sahar
Tulbah
Shamayel Mohammed
Shamayel
Mohammed
Zuhair Rahbeeni
Zuhair
Rahbeeni
Mohammed Alghamdi
Mohammed
Alghamdi
Monther Rababh
Monther
Rababh
Dilek Colak
Dilek
Colak
Namik Kaya
Namik
Kaya
Majid Al-Fayyadh
Majid
Al-Fayyadh
Jehad Alburaiki
Jehad
Alburaiki
Additional file 1: Table S1. of A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy
Springer Nature
2016
Cardiomyopathy
FBXO32
Ubiquitin proteasome system
2016-01-14 05:00:00
Journal contribution
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
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 17Â kb)