X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

Author:

Gedeon A K,Wilson M J,Colley A C,Sillence D O,Mulley J C

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference27 articles.

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2. A new mtDNA mutation in the tRNAL'U-=R gene associated with maternally inherited cardiomyopathy;Silvestri, G.; Santorelli, F.M.; Shanske, S.;Hum Mutat,1994

3. An Xlinked recessive cardiomyopathy with abnormal mitochondria;Neustein, H.B.; Lurie, P.R.; Dahms, B.; Takahashi, M.;Pediatrics,1979

4. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes;Barth, P.G.; Scholte, H.R.; Berden, J.A.;J Neurol Sci,1983

5. Endocardial fibroelastosis: possible X linked inheritance;Hodgson, S.; Child, A.; Dyson, M.;JMed Genet,1987

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