Genotype-phenotype correlation in patients with Usher syndrome and pathogenic variants in MYO7A: implications for future clinical trials.

Saved in:

Bibliographic Details
Title:	Genotype-phenotype correlation in patients with Usher syndrome and pathogenic variants in MYO7A: implications for future clinical trials.
Authors:	Galbis-Martínez L; Department of Genetics, University Hospital Fundacion Jimenez Diaz, IIS-FJD, UAM, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain., Blanco-Kelly F; Department of Genetics, University Hospital Fundacion Jimenez Diaz, IIS-FJD, UAM, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain., García-García G; CIBERER, ISCIII, Madrid, Spain.; Unit of Genetics, University Hospital La Fe - IIS La Fe, Valencia, Spain.; Joint Unit for Rare Diseases IIS La Fe-CIPF, Valencia, Spain., Ávila-Fernández A; Department of Genetics, University Hospital Fundacion Jimenez Diaz, IIS-FJD, UAM, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain., Jaijo T; CIBERER, ISCIII, Madrid, Spain.; Unit of Genetics, University Hospital La Fe - IIS La Fe, Valencia, Spain.; Joint Unit for Rare Diseases IIS La Fe-CIPF, Valencia, Spain., Fuster-García C; CIBERER, ISCIII, Madrid, Spain.; Unit of Genetics, University Hospital La Fe - IIS La Fe, Valencia, Spain.; Joint Unit for Rare Diseases IIS La Fe-CIPF, Valencia, Spain., Perea-Romero I; Department of Genetics, University Hospital Fundacion Jimenez Diaz, IIS-FJD, UAM, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain., Zurita-Muñoz O; Department of Genetics, University Hospital Fundacion Jimenez Diaz, IIS-FJD, UAM, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain., Jimenez-Rolando B; CIBERER, ISCIII, Madrid, Spain.; Department of Ophthalmology, University Hospital Fundacion Jimenez Diaz, IIS-FJD, UAM, Madrid, Spain., Carreño E; CIBERER, ISCIII, Madrid, Spain.; Department of Ophthalmology, University Hospital Fundacion Jimenez Diaz, IIS-FJD, UAM, Madrid, Spain., García-Sandoval B; CIBERER, ISCIII, Madrid, Spain.; Department of Ophthalmology, University Hospital Fundacion Jimenez Diaz, IIS-FJD, UAM, Madrid, Spain., Millán JM; CIBERER, ISCIII, Madrid, Spain.; Unit of Genetics, University Hospital La Fe - IIS La Fe, Valencia, Spain.; Joint Unit for Rare Diseases IIS La Fe-CIPF, Valencia, Spain., Ayuso C; Department of Genetics, University Hospital Fundacion Jimenez Diaz, IIS-FJD, UAM, Madrid, Spain.; CIBERER, ISCIII, Madrid, Spain.
Source:	Acta ophthalmologica [Acta Ophthalmol] 2021 Dec; Vol. 99 (8), pp. 922-930. Date of Electronic Publication: 2021 Feb 11.
Publication Type:	Journal Article; Multicenter Study
Journal Info:	Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101468102 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1755-3768 (Electronic) Linking ISSN: 1755375X NLM ISO Abbreviation: Acta Ophthalmol Subsets: MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1755-3768
DOI:	10.1111/aos.14795