Prenatal Diagnostics in Oxidative Phosphorylation Disorders
Author:
Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/0-387-26992-4_11
Reference25 articles.
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4. Triepels R, van den Heuvel L, Trijbels F et al. Respiratory chain complex 1 deficiency. Am J Med Genet 2001; 106(1):37–45.
5. Hammans SR, Sweeney MG, Brockington M et al. The mitochondrial DNA transfer RNA(Lys)A>G(8344) mutation and the syndrome of myodonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNA. Brain 1993; 116 (Pt3):617–632.
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