ACVR1-activating mutation causes neuropathic pain and sensory neuron hyperexcitability in humans von Yu, Xiaobing, Ton, Amy N., Niu, Zejun, Morales, Blanca M., Chen, Jiadong, Braz, Joao, Lai, Michael H., Barruet, Emilie, Liu, Hongju, Cheung, Kin, Ali, Syed, Chan, Tea, Bigay, Katherine, Ho, Jennifer, Nikolli, Ina, Hansberry, Steven, Wentworth, Kelly, Kriegstein, Arnold, Basbaum, Allan, Hsiao, Edward C.

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Functional Testing of Bone Morphogenetic Protein (BMP) Pathway Variants Identified on Whole‐Exome Sequencing in a Patient with Delayed‐Onset Fibrodysplasia Ossificans Progressiva (... von Wentworth, Kelly L., Lalonde, Robert L., Groppe, Jay C., Brewer, Niambi, Moody, Tania, Hansberry, Steven, Taylor, Kimberly E., Shore, Eileen M., Kaplan, Frederick S., Pignolo, Robert J., Yelick, Pamela C., Hsiao, Edward C.

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An ACVR1 activating mutation causes neuropathic pain and sensory neuron hyperexcitability in humans von Yu, Xiaobing, Ton, Amy N., Niu, Zejun, Morales, Blanca M., Chen, Jiadong, Braz, Joao, Lai, Michael H., Barruet, Emilie, Liu, Hongju, Cheung, Kin, Ali, Syed, Chan, Tea, Bigay, Katherine, Ho, Jennifer, Nikolli, Ina, Hansberry, Steven, Wentworth, Kelly, Kriegstein, Arnold, Basbaum, Allan, Hsiao, Edward C.

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Functional Testing of Bone Morphogenetic Protein (BMP) Pathway Variants Identified on Whole-Exome Sequencing in a Patient with Delayed-Onset Fibrodysplasia Ossificans Progressiva (... von Wentworth, Kelly L, Lalonde, Robert L, Groppe, Jay C, Brewer, Niambi, Moody, Tania, Hansberry, Steven, Taylor, Kimberly E, Shore, Eileen M, Kaplan, Frederick S, Pignolo, Robert J, Yelick, Pamela C, Hsiao, Edward C

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