Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS.

Lopez E, Berenguer M, Tingaud-Sequeira A, Marlin S, Toutain A, Denoyelle F, Picard A, Charron S, Mathieu G, de Belvalet H, Arveiler B, Babin PJ, Lacombe D, Rooryck C

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DOI: 10.1136/jmedgenet-2016-103774
Published: 2016 Nov
Container: Journal of medical genetics
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1136/jmedgenet-2016-103774,
  title = {Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS.},
  author = {Lopez E and Berenguer M and Tingaud-Sequeira A and Marlin S and Toutain A and Denoyelle F and Picard A and Charron S and Mathieu G and de Belvalet H and Arveiler B and Babin PJ and Lacombe D and Rooryck C},
  year = {2016},
  journal = {Journal of medical genetics},
  doi = {10.1136/jmedgenet-2016-103774},
  url = {https://doi.org/10.1136/jmedgenet-2016-103774}
}

RIS

TY  - JOUR
TI  - Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS.
AU  - Lopez E
AU  - Berenguer M
AU  - Tingaud-Sequeira A
AU  - Marlin S
AU  - Toutain A
AU  - Denoyelle F
AU  - Picard A
AU  - Charron S
AU  - Mathieu G
AU  - de Belvalet H
AU  - Arveiler B
AU  - Babin PJ
AU  - Lacombe D
AU  - Rooryck C
PY  - 2016
JO  - Journal of medical genetics
DO  - 10.1136/jmedgenet-2016-103774
UR  - https://doi.org/10.1136/jmedgenet-2016-103774
ER  -

APA

E, L., M, B., A, T., S, M., A, T., F, D., A, P., S, C., G, M., H, D. B., B, A., PJ, B., D, L., & C, R. (2016). Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS.. Journal of medical genetics. https://doi.org/10.1136/jmedgenet-2016-103774

Source records

pubmed · retrieved 2026-09-26T00:57:55.663Z