Pegoraro, E <br/><br/>
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant.  [electronic resource] 

 -  American journal of medical genetics  Feb 1996 
 - 356-62 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/(SICI)1096-8628(19960202)61:4<356::AID-AJMG10>3.0.CO;2-R  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA, Mitochondrial<br/>Dosage Compensation, Genetic<br/>Female<br/>Heterozygote<br/>Humans<br/>Male<br/>Optic Atrophies, Hereditary--diagnosis<br/>Pedigree