Hirano, Motoharu <br/><br/>
Renal complications in a patient with A-to-G mutation of mitochondrial DNA at the 3243 position of leucine tRNA.  [electronic resource] 

 -  Internal medicine (Tokyo, Japan)  Feb 2002 
 - 113-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Review 
<br/><br/><label>ISSN: </label>0918-2918 
<br/><br/><label>Standard No.: </label>10.2169/internalmedicine.41.113  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Atrophy<br/>Biopsy<br/>DNA, Mitochondrial--genetics<br/>Diabetes Mellitus--genetics<br/>Dwarfism--genetics<br/>Female<br/>Fibrosis<br/>Hearing Loss, Bilateral--genetics<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Kidney Diseases--genetics<br/>Kidney Glomerulus--pathology<br/>Mitochondria--ultrastructure<br/>Mitochondrial Diseases--genetics<br/>Point Mutation<br/>RNA, Transfer, Leu--genetics<br/>Syndrome