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Genetic diversity of NDUFV1-dependent mitochondrial complex I deficiency

Medical genomics research performed in diverse population facilitates a better understanding of the genetic basis of developmental disorders, with regional implications for community genetics. Autosomal recessive mitochondrial complex I deficiency (MCID) accounts for a constellation of clinical feat...

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Xehetasun bibliografikoak
Argitaratua izan da:Eur J Hum Genet
Egile Nagusiak: Srivastava, Anshika, Srivastava, Kinshuk Raj, Hebbar, Malavika, Galada, Chelna, Kadavigrere, Rajagopal, Su, Fengyun, Cao, Xuhong, Chinnaiyan, Arul M., Girisha, Katta M., Shukla, Anju, Bielas, Stephanie L.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Springer International Publishing 2018
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6189076/
https://ncbi.nlm.nih.gov/pubmed/29976978
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-018-0209-0
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