Literature DB >> 25775450

Correction: exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies.

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Abstract

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Year:  2015        PMID: 25775450      PMCID: PMC4361588          DOI: 10.1371/journal.pone.0120166

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


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The first author’s name is incorrect in the citation. The correct short name is: González-del Pozo, M. The correct citation is: González-del Pozo, M, Méndez-Vidal C, Bravo-Gil N, Vela-Boza A, Dopazo J, Borrego S, et al. (2014) Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies. PLoS ONE 9(12): e116176. doi:10.1371/journal.pone.0116176
  1 in total

1.  Exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies.

Authors:  María González-del Pozo; Cristina Méndez-Vidal; Nereida Bravo-Gil; Alicia Vela-Boza; Joaquin Dopazo; Salud Borrego; Guillermo Antiñolo
Journal:  PLoS One       Date:  2014-12-29       Impact factor: 3.240

  1 in total

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