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hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction

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hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction. / Chai, Andrea; Withers, James; Koh, Young Ho; Parry, Katherine; Bao, Hong; Zhang, Bing; Budnik, Vivian; Pennetta, Giuseppa.

In: Human Molecular Genetics, Vol. 17, No. 2, 15.01.2008, p. 266-280.

Research output: Contribution to journalArticle

Harvard

Chai, A, Withers, J, Koh, YH, Parry, K, Bao, H, Zhang, B, Budnik, V & Pennetta, G 2008, 'hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction', Human Molecular Genetics, vol. 17, no. 2, pp. 266-280. https://doi.org/10.1093/hmg/ddm303

APA

Chai, A., Withers, J., Koh, Y. H., Parry, K., Bao, H., Zhang, B., Budnik, V., & Pennetta, G. (2008). hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction. Human Molecular Genetics, 17(2), 266-280. https://doi.org/10.1093/hmg/ddm303

Vancouver

Chai A, Withers J, Koh YH, Parry K, Bao H, Zhang B et al. hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction. Human Molecular Genetics. 2008 Jan 15;17(2):266-280. https://doi.org/10.1093/hmg/ddm303

Author

Chai, Andrea ; Withers, James ; Koh, Young Ho ; Parry, Katherine ; Bao, Hong ; Zhang, Bing ; Budnik, Vivian ; Pennetta, Giuseppa. / hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction. In: Human Molecular Genetics. 2008 ; Vol. 17, No. 2. pp. 266-280.