Qiao, Chen <br/><br/>
Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA.  [electronic resource] 

 -  Molecular medicine reports  Aug 2015 
 - 3067-72 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1791-3004 
<br/><br/><label>Standard No.: </label>10.3892/mmr.2015.3714  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Aged<br/>Asian People--genetics<br/>Child<br/>DNA Mutational Analysis<br/>DNA, Mitochondrial--analysis<br/>Female<br/>Haplotypes<br/>Humans<br/>Male<br/>Middle Aged<br/>Mitochondria--genetics<br/>Optic Atrophy, Hereditary, Leber--genetics<br/>Pedigree<br/>Polymorphism, Single Nucleotide