Is the modification of the 13q32.1 regulatory landscape the cause of congenital microcoria?

Authors :: Fares-Taie, L.
Nédelec, B.
David, Pierre
Gerber, S.
Crippa, S.
Passet, Bruno
Vilotte, Jean Luc
Chassaing, N.
Kaplan, J.
Kostic, C.
Calvas, Patrick
Rozet, J. M.
Imagine - Institut des maladies génétiques (IMAGINE - U1163)
Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Department of Ophthalmology
Université de Lausanne (UNIL)
Génétique Animale et Biologie Intégrative (GABI)
Institut National de la Recherche Agronomique (INRA)-AgroParisTech
CHU Toulouse [Toulouse]
Hôpital Universitaire de Toulouse
Source :: Acta Ophthalmologica, European Association for Vision and Eye Research (EVER) Congress, European Association for Vision and Eye Research (EVER) Congress, Oct 2018, Nice, France. pp.1, ⟨10.1111/aos.13972_138⟩
Publication Year :: 2018
Publisher :: HAL CCSD, 2018.
Abstract: National audience

Subjects :: [SDV.GEN]Life Sciences [q-bio]/Genetics
[SDV.GEN.GA]Life Sciences [q-bio]/Genetics/Animal genetics
[SDV]Life Sciences [q-bio]
ComputingMilieux_MISCELLANEOUS

Language :: English
Database :: OpenAIRE
Journal :: Acta Ophthalmologica, European Association for Vision and Eye Research (EVER) Congress, European Association for Vision and Eye Research (EVER) Congress, Oct 2018, Nice, France. pp.1, ⟨10.1111/aos.13972_138⟩
Accession number :: edsair.dedup.wf.001..0f319c9e46bbb0a7135c628734623018
Full Text :: https://doi.org/10.1111/aos.13972_138⟩

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