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Keyword [null mutation]
Result: 1 - 3 | Page: 1 of 1
1.
KCNJ10 Potassium Channel Knockout Abolishes Endocochlear Potential
2.
Null Mutation Of The Fascin2 Gene By TALEN Leading To Progressive Hearing Loss And Retinal Degeneration In C57BL/6J Mice
3.
Novel Human Hormone Sensitive Lipase (HSL) Null Mutation Provides Insight to the Mechanism of Dyslipidemia, Insulin Resistance, and PPARgamma Regulation
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