P4.59 A novel mitochondrial tRNA gene mutation causing PEO present at very low levels in skeletal muscle: implications for molecular diagnosis

2010 ◽  
Vol 20 (9-10) ◽  
pp. 676
Author(s):  
C.L. Alston ◽  
J. Lowe ◽  
D.M. Turnbull ◽  
P. Maddison ◽  
R.W. Taylor
Neurology ◽  
2006 ◽  
Vol 66 (3) ◽  
pp. 447-449 ◽  
Author(s):  
H. Swalwell ◽  
M. Deschauer ◽  
H. Hartl ◽  
M. Strauss ◽  
D. M. Turnbull ◽  
...  

2004 ◽  
Vol 62 (08) ◽  
pp. 149-154 ◽  
Author(s):  
D. Dinour ◽  
S. Mini ◽  
S. Polak-Charcon ◽  
D. Lotan ◽  
E.J. Holtzman

1983 ◽  
Vol 3 (3) ◽  
pp. 371-379
Author(s):  
M Wesolowski ◽  
C Palleschi ◽  
L Frontali ◽  
H Fukuhara

In yeast mitochondria, most of the isoaccepting species of tyrosyl tRNA are coded by a mitochondrial gene, tyrA. A particular isoaccepting species is coded by a second mitochondrial gene, tyrB. This gene is not expressed in certain strains of yeast which show no deficient phenotype. Genetic crosses between strains expressing or not expressing the tyrB gene demonstrate that expression is controlled by specific nuclear genes and that a mutation of the tyrA gene can be bypassed when the tyrB gene is operative.


1984 ◽  
Vol 12 (19) ◽  
pp. 7317-7326 ◽  
Author(s):  
C. Palleschi ◽  
S. Francisci ◽  
M.M. Bianchi ◽  
L. Frontali

1987 ◽  
Vol 15 (18) ◽  
pp. 7381-7394 ◽  
Author(s):  
Rémy Borodonné ◽  
Guy Dirheimer ◽  
Robert P. Martin

1996 ◽  
Vol 90 (s34) ◽  
pp. 16P-16P
Author(s):  
EJ Sherratt ◽  
AW Thomas ◽  
J Gagg ◽  
JC Alcolado ◽  
R Morgan

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