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Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene

Author
Organization
Keywords
OY-PHOS deficiency, mitochondrial encephalopathy, respiratory chain assembly genes, congenital lactic acidosis, Toni Fanconi Debre syndrome, liver cholestasis, C-OXIDASE DEFICIENCY, MITOCHONDRIAL RESPIRATORY-CHAIN, CYTOCHROME-B GENE, REDUCTASE COMPLEX, LEIGH-SYNDROME, PROTEIN, SYSTEM, LIVER, ENCEPHALOPATHY, DISORDERS

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Chicago
De Meirleir, L, S Seneca, E Damis, B Sepulchre, Anne Hoorens, E Gerlo, MTG Silva, EM Hernandez, W Lissens, and Rudy Van Coster. 2003. “Clinical and Diagnostic Characteristics of Complex III Deficiency Due to Mutations in the BCS1L Gene.” American Journal of Medical Genetics Part A 121A (2): 126–131.
APA
De Meirleir, L, Seneca, S., Damis, E., Sepulchre, B., Hoorens, A., Gerlo, E., Silva, M., et al. (2003). Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 121A(2), 126–131.
Vancouver
1.
De Meirleir L, Seneca S, Damis E, Sepulchre B, Hoorens A, Gerlo E, et al. Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2003;121A(2):126–31.
MLA
De Meirleir, L, S Seneca, E Damis, et al. “Clinical and Diagnostic Characteristics of Complex III Deficiency Due to Mutations in the BCS1L Gene.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A 121A.2 (2003): 126–131. Print.
@article{217059,
  author       = {De Meirleir, L and Seneca, S and Damis, E and Sepulchre, B and Hoorens, Anne and Gerlo, E and Silva, MTG and Hernandez, EM and Lissens, W and Van Coster, Rudy},
  issn         = {0148-7299},
  journal      = {AMERICAN JOURNAL OF MEDICAL GENETICS PART A},
  keyword      = {OY-PHOS deficiency,mitochondrial encephalopathy,respiratory chain assembly genes,congenital lactic acidosis,Toni Fanconi Debre syndrome,liver cholestasis,C-OXIDASE DEFICIENCY,MITOCHONDRIAL RESPIRATORY-CHAIN,CYTOCHROME-B GENE,REDUCTASE COMPLEX,LEIGH-SYNDROME,PROTEIN,SYSTEM,LIVER,ENCEPHALOPATHY,DISORDERS},
  language     = {eng},
  number       = {2},
  pages        = {126--131},
  title        = {Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene},
  url          = {http://dx.doi.org/10.1002/ajmg.a.20171},
  volume       = {121A},
  year         = {2003},
}

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