Cecchi, C <br/><br/>
The mottled mouse as a model for human Menkes disease: identification of mutations in the Atp7a gene.  [electronic resource] 

 -  Human molecular genetics  Mar 1997 
 - 425-33 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/6.3.425  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Animals<br/>Carrier Proteins--genetics<br/>Cation Transport Proteins<br/>Copper--metabolism<br/>Copper-Transporting ATPases<br/>DNA Mutational Analysis<br/>DNA Primers--chemistry<br/>Disease Models, Animal<br/>Electrophoresis, Polyacrylamide Gel<br/>Embryo, Mammalian--metabolism<br/>Fluorescence<br/>Heterozygote<br/>Humans<br/>Menkes Kinky Hair Syndrome--genetics<br/>Mice<br/>Mutation<br/>Phenotype<br/>Polymorphism, Genetic<br/>RNA, Messenger--genetics<br/>Recombinant Fusion Proteins<br/>Sequence Analysis<br/>Sequence Deletion<br/>Transcription, Genetic