PUBLICACIÓN

Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications (Scientific Reports, (2021), 11, 1, (1526), 10.1038/s41598-021-81093-y)

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ACCEDER A LA PUBLICACIÓN: Scopus

Perea-Romero I. et al.

2021 Scientific Reports

Multidisciplinary (Q1)

JCR: 4.996

SJR: 1.005

CITAS

6

DOI

10.1038/s41598-021-89275-4

EID

2-s2.0-85105724257

EISSN

2045-2322

AUTORES DE LA UEX

Enrique Galán Gómez

OTRAS PUBLICACIONES DE INTERÉS

The Effect Of Copy Number Variations In Chromosome 16p On Body Weight In Patients With Intellectual Disability
Identification Of Copy-Number Variants In Patients With Overgrowth Disorders
Variability In Phelan-Mcdermid Syndrome In A Cohort Of 210 Individuals
Identification Of Copy-Number Variants In Patients With Overgrowth Disorders
Variability In Phelan-Mcdermid Syndrome In A Cohort Of 210 Individuals
Author Correction: The Utility Of Next Generation Sequencing For Molecular Diagnostics In Rett Syndrome (Scientific Reports, (2017), 7, 1, (12288), 10.1038/s41598-017-11620-3)
Variability In Phelan-Mcdermid Syndrome In A Cohort Of 210 Individuals
Author Correction: The Utility Of Next Generation Sequencing For Molecular Diagnostics In Rett Syndrome (Scientific Reports, (2017), 7, 1, (12288), 10.1038/s41598-017-11620-3)
Author Correction: Genetic Landscape Of 6089 Inherited Retinal Dystrophies Affected Cases In Spain And Their Therapeutic And Extended Epidemiological Implications (Scientific Reports, (2021), 11, 1, (1526), 10.1038/s41598-021-81093-Y)
Author Correction: The Utility Of Next Generation Sequencing For Molecular Diagnostics In Rett Syndrome (Scientific Reports, (2017), 7, 1, (12288), 10.1038/s41598-017-11620-3)
Author Correction: Genetic Landscape Of 6089 Inherited Retinal Dystrophies Affected Cases In Spain And Their Therapeutic And Extended Epidemiological Implications (Scientific Reports, (2021), 11, 1, (1526), 10.1038/s41598-021-81093-Y)
Genetic Landscape Of 6089 Inherited Retinal Dystrophies Affected Cases In Spain And Their Therapeutic And Extended Epidemiological Implications
Author Correction: Genetic Landscape Of 6089 Inherited Retinal Dystrophies Affected Cases In Spain And Their Therapeutic And Extended Epidemiological Implications (Scientific Reports, (2021), 11, 1, (1526), 10.1038/s41598-021-81093-Y)
Genetic Landscape Of 6089 Inherited Retinal Dystrophies Affected Cases In Spain And Their Therapeutic And Extended Epidemiological Implications
Early Clinical And Radiological Improvement In A Young Boy With Metaphyseal Anadysplasia Type 2
Genetic Landscape Of 6089 Inherited Retinal Dystrophies Affected Cases In Spain And Their Therapeutic And Extended Epidemiological Implications
Early Clinical And Radiological Improvement In A Young Boy With Metaphyseal Anadysplasia Type 2
Schuurs–hoeijmakers Syndrome (Pacs1 Neurodevelopmental Disorder): Seven Novel Patients And A Review
Early Clinical And Radiological Improvement In A Young Boy With Metaphyseal Anadysplasia Type 2
Schuurs–hoeijmakers Syndrome (Pacs1 Neurodevelopmental Disorder): Seven Novel Patients And A Review
X Chromosome Inactivation Does Not Necessarily Determine The Severity Of The Phenotype In Rett Syndrome Patients
Schuurs–hoeijmakers Syndrome (Pacs1 Neurodevelopmental Disorder): Seven Novel Patients And A Review
X Chromosome Inactivation Does Not Necessarily Determine The Severity Of The Phenotype In Rett Syndrome Patients
The Effect Of Copy Number Variations In Chromosome 16p On Body Weight In Patients With Intellectual Disability
X Chromosome Inactivation Does Not Necessarily Determine The Severity Of The Phenotype In Rett Syndrome Patients
The Effect Of Copy Number Variations In Chromosome 16p On Body Weight In Patients With Intellectual Disability
Identification Of Copy-Number Variants In Patients With Overgrowth Disorders
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