Disorders of phospholipid metabolism: An emerging class of mitochondrial disease due to defects in nuclear genes

Frontiers in Genetics

Volumn 6, Issue FEB, 2015, Pages

  Lu, Ya Wen ^a   Claypool, Steven M ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Barth syndrome; Cardiolipin; DCMA; Hereditary spastic paraplegia; MEGDEL; Mitochondrial disease; Phospholipid metabolism; Sengers syndrome

Indexed keywords

EID: 84923572321     PISSN: None     EISSN: 16648021     Source Type: Journal    
DOI: 10.3389/fgene.2015.00003     Document Type: Review

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