de Bot, S T <br/><br/>
Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations.  [electronic resource] 

 -  Journal of neurology, neurosurgery, and psychiatry  Oct 2010 
 - 1073-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1468-330X 
<br/><br/><label>Standard No.: </label>10.1136/jnnp.2009.201103  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Aged<br/>Child<br/>Child, Preschool<br/>Female<br/>Genetic Heterogeneity<br/>Genotype<br/>Heterozygote<br/>Humans<br/>Infant<br/>Male<br/>Middle Aged<br/>Mutation<br/>Netherlands<br/>Phenotype<br/>Sensation Disorders--complications<br/>Spastic Paraplegia, Hereditary--complications<br/>Spastin<br/>Tremor--complications