Sudoyo, Herawati <br/><br/>
Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.  [electronic resource] 

 -  Journal of human genetics  2002 
 - 594-604 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1434-5161 
<br/><br/><label>Standard No.: </label>10.1007/s100380200091  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Asia, Southeastern--epidemiology<br/>DNA, Mitochondrial<br/>Female<br/>Haplotypes<br/>Humans<br/>Male<br/>Mitochondria--genetics<br/>Mutation<br/>Optic Atrophy, Hereditary, Leber--epidemiology<br/>Phylogeny<br/>Polymorphism, Single Nucleotide