Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder.
- DOI
- 10.1016/j.ajhg.2021.03.017
- Published
- 2021 May 6
- Container
- American journal of human genetics
- Publisher
- Not recorded
- Open access
- yes
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BibTeX
@article{allodium:10.1016/j.ajhg.2021.03.017,
title = {Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder.},
author = {Latypova X and Vincent M and Mollé A and Adebambo OA and Fourgeux C and Khan TN and Caro A and Rosello M and Orellana C and Niyazov D and Lederer D and Deprez M and Capri Y and Kannu P and Tabet AC and Levy J and Aten E and den Hollander N and Splitt M and Walia J and Immken LL and Stankiewicz P and McWalter K and Suchy S and Louie RJ and Bell S and Stevenson RE and Rousseau J and Willem C and Retiere C and Yang XJ and Campeau PM and Martinez F and Rosenfeld JA and Le Caignec C and Küry S and Mercier S and Moradkhani K and Conrad S and Besnard T and Cogné B and Katsanis N and Bézieau S and Poschmann J and Davis EE and Isidor B},
year = {2021},
journal = {American journal of human genetics},
doi = {10.1016/j.ajhg.2021.03.017},
url = {https://doi.org/10.1016/j.ajhg.2021.03.017}
}RIS
TY - JOUR TI - Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder. AU - Latypova X AU - Vincent M AU - Mollé A AU - Adebambo OA AU - Fourgeux C AU - Khan TN AU - Caro A AU - Rosello M AU - Orellana C AU - Niyazov D AU - Lederer D AU - Deprez M AU - Capri Y AU - Kannu P AU - Tabet AC AU - Levy J AU - Aten E AU - den Hollander N AU - Splitt M AU - Walia J AU - Immken LL AU - Stankiewicz P AU - McWalter K AU - Suchy S AU - Louie RJ AU - Bell S AU - Stevenson RE AU - Rousseau J AU - Willem C AU - Retiere C AU - Yang XJ AU - Campeau PM AU - Martinez F AU - Rosenfeld JA AU - Le Caignec C AU - Küry S AU - Mercier S AU - Moradkhani K AU - Conrad S AU - Besnard T AU - Cogné B AU - Katsanis N AU - Bézieau S AU - Poschmann J AU - Davis EE AU - Isidor B PY - 2021 JO - American journal of human genetics DO - 10.1016/j.ajhg.2021.03.017 UR - https://doi.org/10.1016/j.ajhg.2021.03.017 ER -
APA
X, L., M, V., A, M., OA, A., C, F., TN, K., A, C., M, R., C, O., D, N., D, L., M, D., Y, C., P, K., AC, T., J, L., E, A., N, D. H., M, S., J, W., LL, I., P, S., K, M., S, S., RJ, L., S, B., RE, S., J, R., C, W., C, R., XJ, Y., PM, C., F, M., JA, R., C, L. C., S, K., S, M., K, M., S, C., T, B., B, C., N, K., S, B., J, P., EE, D., & B, I. (2021). Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder.. American journal of human genetics. https://doi.org/10.1016/j.ajhg.2021.03.017
Source records
- pubmed · retrieved 2026-09-25T18:35:33.731Z