All individuals with variants in gene COA6

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AscendingIndividual ID     

ID_report     

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Owner     
00020015 - - - M yes - - 00y01m - - - MC4DN core clinical features: progressive neonatal hypertrophic, cardiomyopathy, lactic acidosis, muscular hypotonia: other features: pulomonary hypertension, persistent ductus arteriosus, dysmorphic features (small chin flat orbital bridges) 1 1 Richard Rodenburg
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