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6. Difficulties and possible solutions in the genetic management of mtDNA disease in the preimplantation embryo. Poulton J; Oakeshott P; Kennedy S Curr Top Dev Biol; 2007; 77():213-25. PubMed ID: 17222705 [TBL] [Abstract][Full Text] [Related]
7. Mitochondrial DNA mutations in human disease. DiMauro S; Schon EA Am J Med Genet; 2001; 106(1):18-26. PubMed ID: 11579421 [TBL] [Abstract][Full Text] [Related]
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9. Clinical presentation of mitochondrial diseases in children with progressive intellectual and neurological deterioration. Sharrard M Dev Med Child Neurol; 2010 May; 52(5):407-8. PubMed ID: 19817774 [No Abstract] [Full Text] [Related]
10. [Pay more attention to the gene diagnosis and functional study to mitochondrial diseases]. Qi Y Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3244-5. PubMed ID: 19159545 [No Abstract] [Full Text] [Related]
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14. Neurologic disorders due to mitochondrial DNA mutations. Debrosse S; Parikh S Semin Pediatr Neurol; 2012 Dec; 19(4):194-202. PubMed ID: 23245552 [TBL] [Abstract][Full Text] [Related]
15. Mitochondrial Disorders of the Nervous System: A Review. Set KK; Sen K; Huq AHM; Agarwal R Clin Pediatr (Phila); 2019 Apr; 58(4):381-394. PubMed ID: 30607979 [No Abstract] [Full Text] [Related]
16. The clinical and audiologic features of mitochondrial hearing loss. Verkerk MM Otolaryngol Head Neck Surg; 2013 Nov; 149(5):795. PubMed ID: 24190890 [No Abstract] [Full Text] [Related]
17. [Molecular diagnosis of mitochondrial DNA deletion]. Murayama K Nihon Rinsho; 2002 Apr; 60 Suppl 4():261-5. PubMed ID: 12013861 [No Abstract] [Full Text] [Related]
18. Ethical issues surrounding the evaluation of oxidative phosphorylation disorders in children. Krawiecki N Semin Neurol; 2001 Sep; 21(3):337-41. PubMed ID: 11641823 [TBL] [Abstract][Full Text] [Related]
19. [Significance of human mitochondrial genome in medicine]. González Moreno O; Novo FJ Rev Med Univ Navarra; 2001; 45(1):29-42. PubMed ID: 11488205 [TBL] [Abstract][Full Text] [Related]