Confirmation ofTENM3involvement in autosomal recessive colobomatous microphthalmia-Reference-Cited by-同舟云学术

Confirmation ofTENM3involvement in autosomal recessive colobomatous microphthalmia

Published:2016-04-22 Issue:7 Volume:170 Page:1895-1898
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Chassaing Nicolas¹²,Ragge Nicola³⁴,Plaisancié Julie¹,Patat Oliver¹,Geneviève David⁵,Rivier François⁶,Malrieu-Eliaou Claudie⁷,Hamel Christian⁸,Kaplan Josseline⁹,Calvas Patrick¹²

Affiliation:

1. CHU Toulouse; Service de Génétique Médicale, Hôpital Purpan; Toulouse France

2. UDEAR; Université de Toulouse, Inserm, UPS, CNRS; Toulouse France

3. Birmingham Women's Hospital Clinical Genetics Unit; Birmingham UK

4. School of Life Sciences; Oxford Brookes University; Oxford UK

5. CHRU Montpellier; Service de Génétique Médicale; Montpellier France

6. CHRU Montpellier; Service de Neuropédiatrie; Montpellier France

7. CHRU Montpellier; Service d'Ophtalmologie; Montpellier France

8. CHRU Montpellier; Maladies Sensorielles Génétiques; Montpellier France

9. Génétique Ophtalmologique INSERM U1163; Paris France

Funder

French Ministry of Health

Fondation Maladies Rare

Retina France patient association

VICTA (Visually Impaired Children Taking Action)

MACS (Microphthalmia, Anophthalmia Children's Society)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference14 articles.

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2. Teneurin-3 specifies morphological and functional connectivity of retinal ganglion cells in the vertebrate visual system;Antinucci;Cell Rep,2013

3. The mammalian Odz gene family: Homologs of a Drosophila pair-rule gene with expression implying distinct yet overlapping developmental roles;Ben-Zur;Dev Biol,2000

4. Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia;Chassaing;Clin Genet,2014

5. Mutations in SOX2 cause anophthalmia;Fantes;Nat Genet,2003

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