Exome sequencing identifies nfs1 deficiency in a novel fe-s cluster disease, infantile mitochondrial complex ii/iii deficiency

Molecular Genetics and Genomic Medicine

Volumn 2, Issue 1, 2014, Pages 73-80

  Farhan, Sali M K ^a,b   Wang, Jian ^a   Robinson, John F ^a   Lahiry, Piya ^a   Siu, Victoria M ^b,c   Prasad, Chitra ^b,c   Kronick, Jonathan B ^d   Ramsay, David A ^c   Anthony Rupar, C ^b,c   Hegele, Robert A ^a,b  

^a ROBARTS RESEARCH INSTITUTE   (Canada)

^b WESTERN UNIVERSITY   (Canada)

^c LONDON HEALTH SCIENCES CENTRE   (Canada)

^d HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Autozygosity mapping; Fe S proteins; Mitochondrial complex deficiency; NFS1; Whole exome sequencing

Indexed keywords

EID: 84902131139     PISSN: None     EISSN: 23249269     Source Type: Journal    
DOI: 10.1002/mgg3.46     Document Type: Article

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