Screening for Autism Spectrum Disorder in Children and Adolescents With Leber's Congenital Amaurosis

Author:

Sallum Juliana Maria FerrazORCID,Pellissari Marina Cruz,Carreiro Luiz Renato,de Vasconcellos Cecília Francini Cabral

Funder

Federal University of Sao Paulo

Publisher

Elsevier BV

Reference52 articles.

1. Ueber Retinitis pigmentosa und angeborene Amaurose;Leber;Albrecht von Graefes Arch Ophthalmol,1869

2. Epidemiology of retinitis pigmentosa in Denmark;Haim;Acta Ophthalmol,2002

3. Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes;Coppieters;Hum Mutat,2010

4. Clinical and molecular findings in a cohort of 152 Brazilian severe early onset inherited retinal dystrophy patients;Sallum;Am J Med Genet C Semin Med Genet,2020

5. Kumaran N, Pennesi ME, Yang P, et al. Leber congenital amaurosis/early-onset severe retinal dystrophy overview (2018 Oct 4 [atualizado em 2023 Mar 23]). In: Adam MP, Feldman J, Mirzaa GM, et al., eds. GeneReviews®. University of Washington, Seattle; 1993-2023. Disponível em: https://www.ncbi.nlm.nih.gov/books/NBK531510/.

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