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RT @DiseaseGenes: RT @FranMartinezGr: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry #Rar…
RT @DiseaseGenes: RT @FranMartinezGr: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry #Rar…
Great collaborative effort! Special thanks to Andrea Cortese for his excellent work. More to come! @UCL_QS_CNMD @UCLIoN @IonSynapse https://t.co/SntCfuN1lR
RT @DiseaseGenes: RT @FranMartinezGr: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry #Rar…
RT @FranMartinezGr: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry #RareDisease #Genetics #morbidgene https://t.co/rXDRMaArMU https://t.co/E2spZTvcl6