Author:
Marchington David R,Scott-Brown Martin,Barlow David H,Poulton Joanna
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference50 articles.
1. Lightowlers R, Chinnery P, Turnbull D, Howell N : Mammalian mitochondrial genetics: hereditary, heteroplasmy and disease. Trends Genet 1997; 13: 450–455.
2. Poulton J, O'Rahilly S, Morten K, Clark A : Mitochondrial DNA, diabetes and pancreatic pathology in Kearns–Sayre syndrome. Diabetologia 1995; 38: 868–871.
3. Weber K, Wilson J, Taylor L, Brierley E, Johnson M, Turnbull D : A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle. Am J Hum Genet 1997; 60: 373–380.
4. Larsson NG, Holme E, Kristiansson B, Oldfors A, Tulinius M : Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome. Pediatr Res 1990; 28: 131–136.
5. Poulton JMA, Pike M, Seller A, Marchington DR, Kennedy S, Brown GK : Advances in genetic management of patients with mitochondrial disease. Dev Med Ch Neurol 2001; 42: 6.
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