Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.

Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Theroux JF, Jefri M, Tanti A, Wu H, Kolobova I, Silviera H, Manzano-Vargas K, Ehresmann S, Hamdan FF, Hettige N, Zhang X, Antonyan L, Nassif C, Ghaloul-Gonzalez L, Sebastian J, Vockley J, Begtrup AG, Wentzensen IM, Crunk A, Nicholls RD, Herman KC, Deignan JL, Al-Hertani W, Efthymiou S, Salpietro V, Miyake N, Makita Y, Matsumoto N, Østern R, Houge G, Hafström M, Fassi E, Houlden H, Klein Wassink-Ruiter JS, Nelson D, Goldstein A, Dabir T, van Gils J, Bourgeron T, Delorme R, Cooper GM, Martinez JE, Finnila CR, Carmant L, Lortie A, Oegema R, van Gassen K, Mehta SG, Huhle D, Abou Jamra R, Martin S, Brunner HG, Lindhout D, Au M, Graham JM Jr, Coubes C, Turecki G, Gravel S, Mechawar N, Rossignol E, Michaud JL, Lessard J, Ernst C, Campeau PM

Open source

DOI
10.1016/j.ajhg.2019.03.022
Published
2019 May 2
Container
American journal of human genetics
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1016/j.ajhg.2019.03.022,
  title = {Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.},
  author = {Bell S and Rousseau J and Peng H and Aouabed Z and Priam P and Theroux JF and Jefri M and Tanti A and Wu H and Kolobova I and Silviera H and Manzano-Vargas K and Ehresmann S and Hamdan FF and Hettige N and Zhang X and Antonyan L and Nassif C and Ghaloul-Gonzalez L and Sebastian J and Vockley J and Begtrup AG and Wentzensen IM and Crunk A and Nicholls RD and Herman KC and Deignan JL and Al-Hertani W and Efthymiou S and Salpietro V and Miyake N and Makita Y and Matsumoto N and Østern R and Houge G and Hafström M and Fassi E and Houlden H and Klein Wassink-Ruiter JS and Nelson D and Goldstein A and Dabir T and van Gils J and Bourgeron T and Delorme R and Cooper GM and Martinez JE and Finnila CR and Carmant L and Lortie A and Oegema R and van Gassen K and Mehta SG and Huhle D and Abou Jamra R and Martin S and Brunner HG and Lindhout D and Au M and Graham JM Jr and Coubes C and Turecki G and Gravel S and Mechawar N and Rossignol E and Michaud JL and Lessard J and Ernst C and Campeau PM},
  year = {2019},
  journal = {American journal of human genetics},
  doi = {10.1016/j.ajhg.2019.03.022},
  url = {https://doi.org/10.1016/j.ajhg.2019.03.022}
}

RIS

TY  - JOUR
TI  - Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.
AU  - Bell S
AU  - Rousseau J
AU  - Peng H
AU  - Aouabed Z
AU  - Priam P
AU  - Theroux JF
AU  - Jefri M
AU  - Tanti A
AU  - Wu H
AU  - Kolobova I
AU  - Silviera H
AU  - Manzano-Vargas K
AU  - Ehresmann S
AU  - Hamdan FF
AU  - Hettige N
AU  - Zhang X
AU  - Antonyan L
AU  - Nassif C
AU  - Ghaloul-Gonzalez L
AU  - Sebastian J
AU  - Vockley J
AU  - Begtrup AG
AU  - Wentzensen IM
AU  - Crunk A
AU  - Nicholls RD
AU  - Herman KC
AU  - Deignan JL
AU  - Al-Hertani W
AU  - Efthymiou S
AU  - Salpietro V
AU  - Miyake N
AU  - Makita Y
AU  - Matsumoto N
AU  - Østern R
AU  - Houge G
AU  - Hafström M
AU  - Fassi E
AU  - Houlden H
AU  - Klein Wassink-Ruiter JS
AU  - Nelson D
AU  - Goldstein A
AU  - Dabir T
AU  - van Gils J
AU  - Bourgeron T
AU  - Delorme R
AU  - Cooper GM
AU  - Martinez JE
AU  - Finnila CR
AU  - Carmant L
AU  - Lortie A
AU  - Oegema R
AU  - van Gassen K
AU  - Mehta SG
AU  - Huhle D
AU  - Abou Jamra R
AU  - Martin S
AU  - Brunner HG
AU  - Lindhout D
AU  - Au M
AU  - Graham JM Jr
AU  - Coubes C
AU  - Turecki G
AU  - Gravel S
AU  - Mechawar N
AU  - Rossignol E
AU  - Michaud JL
AU  - Lessard J
AU  - Ernst C
AU  - Campeau PM
PY  - 2019
JO  - American journal of human genetics
DO  - 10.1016/j.ajhg.2019.03.022
UR  - https://doi.org/10.1016/j.ajhg.2019.03.022
ER  -

APA

S, B., J, R., H, P., Z, A., P, P., JF, T., M, J., A, T., H, W., I, K., H, S., K, M., S, E., FF, H., N, H., X, Z., L, A., C, N., L, G., J, S., J, V., AG, B., IM, W., A, C., RD, N., KC, H., JL, D., W, A., S, E., V, S., N, M., Y, M., N, M., R, Ø., G, H., M, H., E, F., H, H., JS, K. W., D, N., A, G., T, D., J, V. G., T, B., R, D., GM, C., JE, M., CR, F., L, C., A, L., R, O., K, V. G., SG, M., D, H., R, A. J., S, M., HG, B., D, L., M, A., Jr, G. J., C, C., G, T., S, G., N, M., E, R., JL, M., J, L., C, E., & PM, C. (2019). Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.. American journal of human genetics. https://doi.org/10.1016/j.ajhg.2019.03.022

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