Matthews, P M <br/><br/>
Molecular genetic characterization of an X-linked form of Leigh's syndrome.  [electronic resource] 

 -  Annals of neurology  Jun 1993 
 - 652-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0364-5134 
<br/><br/><label>Standard No.: </label>10.1002/ana.410330616  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Aspartic Acid<br/>Base Sequence<br/>Brain Stem--pathology<br/>Cells, Cultured<br/>Cesarean Section<br/>Citrate (si)-Synthase--metabolism<br/>DNA--genetics<br/>Exons<br/>Fibroblasts--pathology<br/>Gestational Age<br/>Humans<br/>Infant, Newborn<br/>Leigh Disease--genetics<br/>Leukocytes--physiology<br/>Male<br/>Mitochondria, Heart--enzymology<br/>Mitochondria, Liver--enzymology<br/>Molecular Sequence Data<br/>Necrosis<br/>Oligodeoxyribonucleotides<br/>Point Mutation<br/>Pyruvate Dehydrogenase Complex--genetics<br/>Skin--pathology<br/>X Chromosome