Mutation of zebrafish dihydrolipoamide branched-chain transacylase E2 results in motor dysfunction and models maple syrup urine disease

SUMMARY Analysis of zebrafish mutants that demonstrate abnormal locomotive behavior can elucidate the molecular requirements for neural network function and provide new models of human disease. Here, we show that zebrafish quetschkommode (que) mutant larvae exhibit a progressive locomotor defect tha...

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Bibliographic Details
Main Authors: Timo Friedrich (Author), Aaron M. Lambert (Author), Mark A. Masino (Author), Gerald B. Downes (Author)
Format: Book
Published: The Company of Biologists, 2012-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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