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CORRIGENDUM: The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations.

Chen, C-A; Bosch, DGM; Cho ScM, MT; Rosenfeld, JA; Shinawi, M; Lewis, RA; Mann, J; Jayakar, P; Payne, K; Walsh, L; et al. Chen, C-A; Bosch, DGM; Cho ScM, MT; Rosenfeld, JA; Shinawi, M; Lewis, RA; Mann, J; Jayakar, P; Payne, K; Walsh, L; Moss, T; Schreiber, A; Schoonveld, C; Monaghan, KG; Elmslie, F; Douglas, G; Boonstra, FN; Millan, F; Cremers, FPM; McKnight, D; Richard, G; Juusola, J; Kendall, F; Ramsey, K; Anyane-Yeboa, K; Malkin, E; Chung, WK; Niyazov, D; Pascual, JM; Walkiewicz, M; Veluchamy, V; Li, C; Hisama, FM; de Vries, BBA; Schaaf, C (2017) CORRIGENDUM: The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations. Genet Med, 19 (8). p. 962. ISSN 1530-0366 https://doi.org/10.1038/gim.2017.12
SGUL Authors: Elmslie, Frances

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Abstract

This corrects the article DOI: 10.1038/gim.2016.18.

Item Type: Article
Additional Information: This is a post-peer-review, pre-copyedit version of an article published in Genetics in Medicine. The final authenticated version is available online at: http://dx.doi.org/10.1038/gim.2017.12
Keywords: Genetics & Heredity, 0604 Genetics, 1103 Clinical Sciences
Journal or Publication Title: Genet Med
ISSN: 1530-0366
Language: eng
Dates:
DateEvent
4 August 2017Published
Publisher License: Publisher's own licence
PubMed ID: 28777376
Go to PubMed abstract
URI: http://sgultest.da.ulcc.ac.uk/id/eprint/110124
Publisher's version: https://doi.org/10.1038/gim.2017.12

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