Lucienne, Marie <br/><br/>
In-depth phenotyping reveals common and novel disease symptoms in a hemizygous knock-in mouse model (Mut-ko/ki) of mut-type methylmalonic aciduria.  [electronic resource] 

 -  Biochimica et biophysica acta. Molecular basis of disease  03 2020 
 - 165622 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1879-260X 
<br/><br/><label>Standard No.: </label>10.1016/j.bbadis.2019.165622  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Metabolism, Inborn Errors--genetics<br/>Animals<br/>Anxiety--genetics<br/>Bone Density--genetics<br/>Disease Models, Animal<br/>Female<br/>Kidney--pathology<br/>Male<br/>Methylmalonic Acid--metabolism<br/>Methylmalonyl-CoA Mutase--deficiency<br/>Mice<br/>Phenotype