Matesic, L E <br/><br/>
Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Aug 2001 
 - 10238-43 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.181336698  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing<br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>Carrier Proteins--genetics<br/>Chromosome Mapping<br/>Chromosomes, Artificial, Bacterial--genetics<br/>DNA Primers--genetics<br/>Genetic Complementation Test<br/>Melanosomes--metabolism<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Mutant Strains<br/>Molecular Sequence Data<br/>Multigene Family<br/>Mutation<br/>Pigmentation Disorders--genetics<br/>Sequence Homology, Amino Acid<br/>rab GTP-Binding Proteins--genetics<br/>rab27 GTP-Binding Proteins