Point mutation of the mitochondrial tRNA<sup>Leu</sup> gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.

MANOUVRIER S; ROETIG A; HANNEBIQUE G; GHEERBRANDT J-D; ROYER-LEGRAIN G; MUNNICH A; PARENT M; GRUENFELD J-P; BONNEFONT J-P

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J-GLOBAL ID：200902191378657654 Reference number：95A0782569

Point mutation of the mitochondrial tRNA^Leu gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.

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Material：
Volume： 32 Issue： 8 Page： 654-656 Publication year： Aug. 1995
JST Material Number： T0190A ISSN： 0022-2593 Document type： Article
Country of issue： United Kingdom (GBR) Language： ENGLISH (EN)

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Point mutation of the mitochondrial tRNALeu gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.

Point mutation of the mitochondrial tRNA^Leu gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.