Labay, V <br/><br/>
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness.  [electronic resource] 

 -  Nature genetics  Jul 1999 
 - 300-4 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/10372  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Anemia, Megaloblastic--complications<br/>Animals<br/>Base Sequence<br/>Carrier Proteins--genetics<br/>Cricetinae<br/>DNA--genetics<br/>DNA Primers--genetics<br/>Deafness--complications<br/>Diabetes Complications<br/>Diabetes Mellitus--genetics<br/>Female<br/>Genes, Recessive<br/>Genetic Markers<br/>Humans<br/>Male<br/>Membrane Transport Proteins<br/>Mice<br/>Molecular Sequence Data<br/>Mutation<br/>Physical Chromosome Mapping<br/>Sequence Homology, Amino Acid<br/>Syndrome<br/>Thiamine--metabolism