New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset - Concepedia

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New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset

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Citations

19

References

2012

Year

María del Mar O’Callaghan, Sonia Emperador, Ester López‐Gallardo, Cristina Jou, Núria Bujan, Raquel Montero, Àngels García‐Cazorla, Diana Gonzaga, Isidró Ferrer, Paz Briones,

BiologyMendelian DisorderMitochondrial BiogenesisMitochondrial FunctionGenetic DisorderNatural SciencesGeneticsMolecular BiologyDna ReplicationMitochondrial MedicineMolecular GeneticsChildhood OnsetMedicineSevere Encephalopamyopathic PhenotypesClinical Genetics

References

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