Publication | Closed Access
Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation
49
Citations
25
References
1994
Year
Clinical SymptomsMendelian DisorderMelas FamilyMedicineGeneticsExtreme VariabilityGenetic DisorderPathologyMolecular GeneticsDisease Gene IdentificationGenomicsMolecular DiagnosticsClinical Genetics
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