Schwartz, Charles E <br/><br/>
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene.  [electronic resource] 

 -  American journal of human genetics  Jul 2005 
 - 41-53 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/431313  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, X<br/>Developmental Disabilities--genetics<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>X-Linked Intellectual Disability--genetics<br/>Middle Aged<br/>Monocarboxylic Acid Transporters--genetics<br/>Muscle Weakness--genetics<br/>Mutation<br/>Paraplegia--genetics<br/>Pedigree<br/>Symporters