Identical Mitochondrial DNA Deletion in a Woman with Ocular Myopathy and in Her Son with Pearson Syndrome-Reference-Cited by-同舟云学术

Identical Mitochondrial DNA Deletion in a Woman with Ocular Myopathy and in Her Son with Pearson Syndrome

Published:2002-09 Issue:3 Volume:71 Page:679-683
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Shanske Sara,Tang Yingying,Hirano Michio,Nishigaki Yutaka,Tanji Kurenai,Bonilla Eduardo,Sue Carolyn,Krishna Sindu,Carlo Jose R.,Willner Judith,Schon Eric A.,DiMauro Salvatore

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference21 articles.

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2. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981

3. Mitochondrial diabetes revisited;Ballinger;Nat Genet,1994

4. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion;Ballinger;Nat Genet,1992

5. Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome;Bernes;J Pediatr,1993

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