Rogers, R Curtis <br/><br/>
Finding new etiologies of mental retardation and hypotonia: X marks the spot.  [electronic resource] 

 -  Developmental medicine and child neurology  Feb 2008 
 - 104-11 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>0012-1622 
<br/><br/><label>Standard No.: </label>10.1111/j.1469-8749.2007.02022.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Chromosomes, Human, X<br/>Humans<br/>Membrane Transport Proteins--deficiency<br/>X-Linked Intellectual Disability--genetics<br/>Methyl-CpG-Binding Protein 2--genetics<br/>Monocarboxylic Acid Transporters--genetics<br/>Muscle Hypotonia--genetics<br/>Muscle Spasticity--genetics<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Plasma Membrane Neurotransmitter Transport Proteins--genetics<br/>Sex Chromosome Disorders--diagnosis<br/>Spermine Synthase--deficiency<br/>Symporters<br/>alpha-Thalassemia--diagnosis