Citations for

1	MTCMH5D
	Maternally inherited cardiomyopathy : a new phenotype associated with the A to G at nt.3243 of mitochondrial DNA (melas mutation).
	Silvestri G, et al.
	Muscle Nerve 20 : 221-225. 1997
2	MTCMH5D
	The mitochondrial A3243G mutation presenting as severe cardiomyopathy.
	Vilarinho L, Santorelli FM, Rosas MJ, Tavares C, Melo-Pires M, DiMauro S.
	J Med Genet 34(7):607-9. 1997
3	MTCMH5D
	A novel combination of mitochondrial tRNA and ND1 gene mutations in a syndrome with MELAS, cardiomyopathy, and diabetes mellitus.
	Jaksch M, et al.
	Hum Mutat 7 : 358-360. 1996
4	MTCMH5D
	Point mutation of the mitochondrial tRNALeu gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.
	Manouvrier S, Rotig A, Hannebique G, Gheerbrandt JD, Royer-Legrain G, Munnich A, Parent M, Grunfeld JP, Largilliere C, Lombes A, et al.
	J Med Genet 32 : 654-656. 1995
5	DMD, MTCMH5D
	Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy.
	Muntoni F, et al.
	Am J Hum Genet 56 : 151-157. 1995