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Whole-Exome Sequencing of 24 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Keratoconus.
González-Atienza, Carmen; Sánchez-Cazorla, Eloísa; Villoldo-Fernández, Natalia; Del Hierro, Almudena; Boto, Ana; Guerrero-Carretero, Marta; Nieves-Moreno, María; Arruti, Natalia; Rodríguez-Solana, Patricia; Mena, Rocío; Rodríguez-Jiménez, Carmen; Rosa-Pérez, Irene; Acal, Juan Carlos; Blasco, Joana; Naranjo-Castresana, Marta; Ruz-Caracuel, Beatriz; Montaño, Victoria E F; Ortega Patrón, Cristina; Rubio-Martín, M Esther; García-Fernández, Laura; Rikeros-Orozco, Emi; Gómez-Cano, María de Los Ángeles; Delgado-Mora, Luna; Noval, Susana; Vallespín, Elena.
  • González-Atienza C; Molecular Ophthalmology Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Sánchez-Cazorla E; Molecular Ophthalmology Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Villoldo-Fernández N; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Del Hierro A; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Boto A; European Reference Network on Eye Diseases (ERN-EYE), Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Guerrero-Carretero M; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Nieves-Moreno M; European Reference Network on Eye Diseases (ERN-EYE), Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Arruti N; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Rodríguez-Solana P; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Mena R; European Reference Network on Eye Diseases (ERN-EYE), Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Rodríguez-Jiménez C; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Rosa-Pérez I; European Reference Network on Eye Diseases (ERN-EYE), Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Acal JC; Molecular Ophthalmology Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Blasco J; Molecular Ophthalmology Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Naranjo-Castresana M; Biomedical Research Center in the Rare Diseases Network (CIBERER), Carlos II Health Institute (ISCIII), 28029 Madrid, Spain.
  • Ruz-Caracuel B; Molecular Ophthalmology Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Montaño VEF; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Ortega Patrón C; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Rubio-Martín ME; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • García-Fernández L; Department of Pediatric Ophthalmology, IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Rikeros-Orozco E; Biomedical Research Center in the Rare Diseases Network (CIBERER), Carlos II Health Institute (ISCIII), 28029 Madrid, Spain.
  • Gómez-Cano MLÁ; Clinical Bioinformatics Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, CIBERER, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Delgado-Mora L; Molecular Ophthalmology Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Noval S; Biomedical Research Center in the Rare Diseases Network (CIBERER), Carlos II Health Institute (ISCIII), 28029 Madrid, Spain.
  • Vallespín E; Molecular Ophthalmology Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, Hospital Universitario La Paz, 28046 Madrid, Spain.
Genes (Basel) ; 14(10)2023 09 22.
Article en En | MEDLINE | ID: mdl-37895187
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Distrofias Hereditarias de la Córnea / Queratocono Límite: Child / Humans Idioma: En Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Distrofias Hereditarias de la Córnea / Queratocono Límite: Child / Humans Idioma: En Año: 2023 Tipo del documento: Article