Mitochondrial involvement in a Bosch-Boonstra-Schaaf optic atrophy syndrome patient with a novel de novo NR2F1 gene mutation-Reference-Cited by-同舟云学术

Mitochondrial involvement in a Bosch-Boonstra-Schaaf optic atrophy syndrome patient with a novel de novo NR2F1 gene mutation

Published:2018-02-06 Issue:4 Volume:63 Page:525-528
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Martín-Hernández Elena,Rodríguez-García María Elena,Chen Chun-An,Cotrina-Vinagre Francisco Javier,Carnicero-Rodríguez Patricia,Bellusci Marcello,Schaaf Christian P.^ORCID,Martínez-Azorín Francisco^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/s10038-017-0398-3.pdf

Reference16 articles.

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3. Tang K, Tsai SY, Tsai MJ. COUP-TFs and eye development. Biochim Biophys Acta. 2015;1849:201–9. https://doi.org/10.1016/j.bbagrm.2014.05.022 .

4. Flore G, et al. Gradient COUP-TFI Expression is required for functional organization of the hippocampal septo-temporal longitudinal axis. Cereb Cortex. 2017;27:1629–43. https://doi.org/10.1093/cercor/bhv336 .

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