Rare and de novo coding variants in chromodomain genes in Chiari I malformation.

Sadler B, Wilborn J, Antunes L, Kuensting T, Hale AT, Gannon SR, McCall K, Cruchaga C, Harms M, Voisin N, Reymond A, Cappuccio G, Brunetti-Pierri N, Tartaglia M, Niceta M, Leoni C, Zampino G, Ashley-Koch A, Urbizu A, Garrett ME, Soldano K, Macaya A, Conrad D, Strahle J, Dobbs MB, Turner TN, Shannon CN, Brockmeyer D, Limbrick DD, Gurnett CA, Haller G.

Open source

DOI
10.1016/j.ajhg.2020.12.001
Published
2020-12-21
Container
Am J Hum Genet
Publisher
Not recorded
Open access
no

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BibTeX

@article{allodium:10.1016/j.ajhg.2020.12.001,
  title = {Rare and de novo coding variants in chromodomain genes in Chiari I malformation.},
  author = {Sadler B and  Wilborn J and  Antunes L and  Kuensting T and  Hale AT and  Gannon SR and  McCall K and  Cruchaga C and  Harms M and  Voisin N and  Reymond A and  Cappuccio G and  Brunetti-Pierri N and  Tartaglia M and  Niceta M and  Leoni C and  Zampino G and  Ashley-Koch A and  Urbizu A and  Garrett ME and  Soldano K and  Macaya A and  Conrad D and  Strahle J and  Dobbs MB and  Turner TN and  Shannon CN and  Brockmeyer D and  Limbrick DD and  Gurnett CA and  Haller G.},
  year = {2021},
  journal = {Am J Hum Genet},
  doi = {10.1016/j.ajhg.2020.12.001},
  url = {https://doi.org/10.1016/j.ajhg.2020.12.001}
}

RIS

TY  - JOUR
TI  - Rare and de novo coding variants in chromodomain genes in Chiari I malformation.
AU  - Sadler B
AU  -  Wilborn J
AU  -  Antunes L
AU  -  Kuensting T
AU  -  Hale AT
AU  -  Gannon SR
AU  -  McCall K
AU  -  Cruchaga C
AU  -  Harms M
AU  -  Voisin N
AU  -  Reymond A
AU  -  Cappuccio G
AU  -  Brunetti-Pierri N
AU  -  Tartaglia M
AU  -  Niceta M
AU  -  Leoni C
AU  -  Zampino G
AU  -  Ashley-Koch A
AU  -  Urbizu A
AU  -  Garrett ME
AU  -  Soldano K
AU  -  Macaya A
AU  -  Conrad D
AU  -  Strahle J
AU  -  Dobbs MB
AU  -  Turner TN
AU  -  Shannon CN
AU  -  Brockmeyer D
AU  -  Limbrick DD
AU  -  Gurnett CA
AU  -  Haller G.
PY  - 2021
JO  - Am J Hum Genet
DO  - 10.1016/j.ajhg.2020.12.001
UR  - https://doi.org/10.1016/j.ajhg.2020.12.001
ER  -

APA

B, S., J, W., L, A., T, K., AT, H., SR, G., K, M., C, C., M, H., N, V., A, R., G, C., N, B., M, T., M, N., C, L., G, Z., A, A., A, U., ME, G., K, S., A, M., D, C., J, S., MB, D., TN, T., CN, S., D, B., DD, L., CA, G., & G., H. (2021). Rare and de novo coding variants in chromodomain genes in Chiari I malformation.. Am J Hum Genet. https://doi.org/10.1016/j.ajhg.2020.12.001

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