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Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice
Deafness in spontaneously occurring mouse mutants is often associated with defects in cochlea sensory hair cells, opening an avenue to systematically identify genes critical for hair cell structure and function. The classical semidominant mouse mutant varitint-waddler (Va) exhibits early-onset heari...
में बचाया:
| मुख्य लेखकों: | , , , , , |
|---|---|
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
National Academy of Sciences
2002
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC137533/ https://ncbi.nlm.nih.gov/pubmed/12403827 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.222425399 |
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