Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder.

Latypova X, Vincent M, Mollé A, Adebambo OA, Fourgeux C, Khan TN, Caro A, Rosello M, Orellana C, Niyazov D, Lederer D, Deprez M, Capri Y, Kannu P, Tabet AC, Levy J, Aten E, den Hollander N, Splitt M, Walia J, Immken LL, Stankiewicz P, McWalter K, Suchy S, Louie RJ, Bell S, Stevenson RE, Rousseau J, Willem C, Retiere C, Yang XJ, Campeau PM, Martinez F, Rosenfeld JA, Le Caignec C, Küry S, Mercier S, Moradkhani K, Conrad S, Besnard T, Cogné B, Katsanis N, Bézieau S, Poschmann J, Davis EE, Isidor B

Open source

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

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