Ragothaman, Mona <br/><br/>
Complex phenotypes in an Indian family with homozygous SCA2 mutations.  [electronic resource] 

 -  Annals of neurology  Jan 2004 
 - 130-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0364-5134 
<br/><br/><label>Standard No.: </label>10.1002/ana.10815  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Ataxia--genetics<br/>Ataxins<br/>DNA Mutational Analysis<br/>DNA Repeat Expansion<br/>Homozygote<br/>Humans<br/>India<br/>Male<br/>Middle Aged<br/>Nerve Tissue Proteins<br/>Parkinsonian Disorders--genetics<br/>Pedigree<br/>Phenotype<br/>Proteins--genetics<br/>Retinitis Pigmentosa--genetics