SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance.
- DOI
- 10.1093/hmg/ddac114
- Published
- 2022 Sep 29
- Container
- Human molecular genetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1093/hmg/ddac114,
title = {SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance.},
author = {Cordovado A and Schaettin M and Jeanne M and Panasenkava V and Denommé-Pichon AS and Keren B and Mignot C and Doco-Fenzy M and Rodan L and Ramsey K and Narayanan V and Jones JR and Prijoles EJ and Mitchell WG and Ozmore JR and Juliette K and Torti E and Normand EA and Granger L and Petersen AK and Au MG and Matheny JP and Phornphutkul C and Chambers MK and Fernández-Ramos JA and López-Laso E and Kruer MC and Bakhtiari S and Zollino M and Morleo M and Marangi G and Mei D and Pisano T and Guerrini R and Louie RJ and Childers A and Everman DB and Isidor B and Audebert-Bellanger S and Odent S and Bonneau D and Gilbert-Dussardier B and Redon R and Bézieau S and Laumonnier F and Stoeckli ET and Toutain A and Vuillaume ML},
year = {2022},
journal = {Human molecular genetics},
doi = {10.1093/hmg/ddac114},
url = {https://doi.org/10.1093/hmg/ddac114}
}RIS
TY - JOUR TI - SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance. AU - Cordovado A AU - Schaettin M AU - Jeanne M AU - Panasenkava V AU - Denommé-Pichon AS AU - Keren B AU - Mignot C AU - Doco-Fenzy M AU - Rodan L AU - Ramsey K AU - Narayanan V AU - Jones JR AU - Prijoles EJ AU - Mitchell WG AU - Ozmore JR AU - Juliette K AU - Torti E AU - Normand EA AU - Granger L AU - Petersen AK AU - Au MG AU - Matheny JP AU - Phornphutkul C AU - Chambers MK AU - Fernández-Ramos JA AU - López-Laso E AU - Kruer MC AU - Bakhtiari S AU - Zollino M AU - Morleo M AU - Marangi G AU - Mei D AU - Pisano T AU - Guerrini R AU - Louie RJ AU - Childers A AU - Everman DB AU - Isidor B AU - Audebert-Bellanger S AU - Odent S AU - Bonneau D AU - Gilbert-Dussardier B AU - Redon R AU - Bézieau S AU - Laumonnier F AU - Stoeckli ET AU - Toutain A AU - Vuillaume ML PY - 2022 JO - Human molecular genetics DO - 10.1093/hmg/ddac114 UR - https://doi.org/10.1093/hmg/ddac114 ER -
APA
A, C., M, S., M, J., V, P., AS, D., B, K., C, M., M, D., L, R., K, R., V, N., JR, J., EJ, P., WG, M., JR, O., K, J., E, T., EA, N., L, G., AK, P., MG, A., JP, M., C, P., MK, C., JA, F., E, L., MC, K., S, B., M, Z., M, M., G, M., D, M., T, P., R, G., RJ, L., A, C., DB, E., B, I., S, A., S, O., D, B., B, G., R, R., S, B., F, L., ET, S., A, T., & ML, V. (2022). SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance.. Human molecular genetics. https://doi.org/10.1093/hmg/ddac114
Source records
- pubmed · retrieved 2026-09-27T10:31:51.368Z