De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder.

Gregor A, Sadleir LG, Asadollahi R, Azzarello-Burri S, Battaglia A, Ousager LB, Boonsawat P, Bruel AL, Buchert R, Calpena E, Cogné B, Dallapiccola B, Distelmaier F, Elmslie F, Faivre L, Haack TB, Harrison V, Henderson A, Hunt D, Isidor B, Joset P, Kumada S, Lachmeijer AMA, Lees M, Lynch SA, Martinez F, Matsumoto N, McDougall C, Mefford HC, Miyake N, Myers CT, Moutton S, Nesbitt A, Novelli A, Orellana C, Rauch A, Rosello M, Saida K, Santani AB, Sarkar A, Scheffer IE, Shinawi M, Steindl K, Symonds JD, Zackai EH, University of Washington Center for Mendelian Genomics, DDD Study, Reis A, Sticht H, Zweier C

Open source

DOI
10.1016/j.ajhg.2018.07.003
Published
2018 Aug 2
Container
American journal of human genetics
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1016/j.ajhg.2018.07.003,
  title = {De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder.},
  author = {Gregor A and Sadleir LG and Asadollahi R and Azzarello-Burri S and Battaglia A and Ousager LB and Boonsawat P and Bruel AL and Buchert R and Calpena E and Cogné B and Dallapiccola B and Distelmaier F and Elmslie F and Faivre L and Haack TB and Harrison V and Henderson A and Hunt D and Isidor B and Joset P and Kumada S and Lachmeijer AMA and Lees M and Lynch SA and Martinez F and Matsumoto N and McDougall C and Mefford HC and Miyake N and Myers CT and Moutton S and Nesbitt A and Novelli A and Orellana C and Rauch A and Rosello M and Saida K and Santani AB and Sarkar A and Scheffer IE and Shinawi M and Steindl K and Symonds JD and Zackai EH and University of Washington Center for Mendelian Genomics and DDD Study and Reis A and Sticht H and Zweier C},
  year = {2018},
  journal = {American journal of human genetics},
  doi = {10.1016/j.ajhg.2018.07.003},
  url = {https://doi.org/10.1016/j.ajhg.2018.07.003}
}

RIS

TY  - JOUR
TI  - De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder.
AU  - Gregor A
AU  - Sadleir LG
AU  - Asadollahi R
AU  - Azzarello-Burri S
AU  - Battaglia A
AU  - Ousager LB
AU  - Boonsawat P
AU  - Bruel AL
AU  - Buchert R
AU  - Calpena E
AU  - Cogné B
AU  - Dallapiccola B
AU  - Distelmaier F
AU  - Elmslie F
AU  - Faivre L
AU  - Haack TB
AU  - Harrison V
AU  - Henderson A
AU  - Hunt D
AU  - Isidor B
AU  - Joset P
AU  - Kumada S
AU  - Lachmeijer AMA
AU  - Lees M
AU  - Lynch SA
AU  - Martinez F
AU  - Matsumoto N
AU  - McDougall C
AU  - Mefford HC
AU  - Miyake N
AU  - Myers CT
AU  - Moutton S
AU  - Nesbitt A
AU  - Novelli A
AU  - Orellana C
AU  - Rauch A
AU  - Rosello M
AU  - Saida K
AU  - Santani AB
AU  - Sarkar A
AU  - Scheffer IE
AU  - Shinawi M
AU  - Steindl K
AU  - Symonds JD
AU  - Zackai EH
AU  - University of Washington Center for Mendelian Genomics
AU  - DDD Study
AU  - Reis A
AU  - Sticht H
AU  - Zweier C
PY  - 2018
JO  - American journal of human genetics
DO  - 10.1016/j.ajhg.2018.07.003
UR  - https://doi.org/10.1016/j.ajhg.2018.07.003
ER  -

APA

A, G., LG, S., R, A., S, A., A, B., LB, O., P, B., AL, B., R, B., E, C., B, C., B, D., F, D., F, E., L, F., TB, H., V, H., A, H., D, H., B, I., P, J., S, K., AMA, L., M, L., SA, L., F, M., N, M., C, M., HC, M., N, M., CT, M., S, M., A, N., A, N., C, O., A, R., M, R., K, S., AB, S., A, S., IE, S., M, S., K, S., JD, S., EH, Z., Genomics, U. O. W. C. F. M., Study, D., A, R., H, S., & C, Z. (2018). De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder.. American journal of human genetics. https://doi.org/10.1016/j.ajhg.2018.07.003

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