The A to G transition at nt.3243 of the tRNA(Leu(UUR)) gene of mtDNA, commonly associated with MELAS, was detected in several members of a family affected by a maternally inherited form of hypertrophic cardiomyopathy. These findings suggest adding cardiomyopathy in the list of phenotypes associated with the 3243 mutation.

Silvestri, G., Bertini, E., Servidei, S., Rana, M., Zachara, E., Ricci, E., Tonali, P., Maternally inherited cardiomyopathy: A new phenotype associated with the A to G at nt.3243 of mitochondrial DNA (MELAS mutation), <<MUSCLE & NERVE>>, 1997; 20 (2): 221-225. [doi:10.1002/(SICI)1097-4598(199702)20:2<221::AID-MUS13>3.0.CO;2-5] [http://hdl.handle.net/10807/166585]

Maternally inherited cardiomyopathy: A new phenotype associated with the A to G at nt.3243 of mitochondrial DNA (MELAS mutation)

Silvestri, Gabriella;Servidei, Serenella;Ricci, Enzo;
1997

Abstract

The A to G transition at nt.3243 of the tRNA(Leu(UUR)) gene of mtDNA, commonly associated with MELAS, was detected in several members of a family affected by a maternally inherited form of hypertrophic cardiomyopathy. These findings suggest adding cardiomyopathy in the list of phenotypes associated with the 3243 mutation.
1997
Inglese
Silvestri, G., Bertini, E., Servidei, S., Rana, M., Zachara, E., Ricci, E., Tonali, P., Maternally inherited cardiomyopathy: A new phenotype associated with the A to G at nt.3243 of mitochondrial DNA (MELAS mutation), <<MUSCLE & NERVE>>, 1997; 20 (2): 221-225. [doi:10.1002/(SICI)1097-4598(199702)20:2<221::AID-MUS13>3.0.CO;2-5] [http://hdl.handle.net/10807/166585]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/166585
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