Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Andrew M. M. Morris"'
Autor:
Stephanie Grunewald, Cathy E. Woodward, Lara Abulhoul, Peter E. Clayton, Shamima Rahman, Michael G. Hanna, Joanna Poulton, James V. Leonard, Mary G. Sweeney, Carl Fratter, Alexander Broomfield, Andrew M. M. Morris
Publikováno v:
Journal of Inherited Metabolic Disease
Background Single large-scale mitochondrial DNA (mtDNA) deletions (SLSMDs) are amongst the most frequently diagnosed mtDNA disorders in childhood, yet their natural history remains poorly understood. We report the natural history of a large multicent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::987c4ad642cc27dc95d35a01fdbf0b9d
https://pubmed.ncbi.nlm.nih.gov/25352051
https://pubmed.ncbi.nlm.nih.gov/25352051
Autor:
R. George F. Gray, Julian Blake, Jan-Willem Taanman, James V. Leonard, Patrick J. McKiernan, Andrew M. M. Morris, Anthony H.V. Schapira, J. Mark Cooper
Publikováno v:
The American Journal of Pathology. 155:67-70
Mitochondrial DNA depletion syndrome is an autosomal inherited disease associated with grossly reduced cellular levels of mitochondrial DNA in infancy. Most patients are born after a full and uncomplicated pregnancy, are normal at birth, but develop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::179e494ac8bd407ce3d8c63c78080b35
https://doi.org/10.1016/s0002-9440(10)65100-0
https://doi.org/10.1016/s0002-9440(10)65100-0