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Absence of Platelet Phenotype in Mice Lacking the Motor Protein Myosin Va
BACKGROUND: The motor protein myosin Va plays an important role in the trafficking of intracellular vesicles. Mutation of the Myo5a gene causes Griscelli syndrome type 1 in humans and the dilute phenotype in mice, which are both characterised by pigment dilution and neurological defects as a result...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3548825/ https://ncbi.nlm.nih.gov/pubmed/23349704 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0053239 |
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