Usher Syndrome Latest Advances

Mouse models and translational research progress of hereditary vestibular dysfunction.

Journal: Journal of vestibular research : equilibrium & orientation

Published: May 30, 2026

A regulatory axis for tonotopic MYO7A expression in cochlear hair cells.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: April 07, 2026

Identification of a recessive PCDH15 nonsense variant in purebred goats with vestibular dysfunction.

Journal: Veterinary and animal science

Published: March 30, 2026

Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population-Specific Variants and Clinical Correlations.

Journal: Clinical genetics

Published: March 18, 2026

Somatic mosaicism of a novel USH2A variant in Usher syndrome.

Journal: Ophthalmic genetics

Published: March 10, 2026

Heimler Syndrome Caused by Novel PEX6 Variants: Clinical and Genetic Characterization in a Saudi Cohort.

Journal: Genes

Published: March 05, 2026

Molecular Characterization of Syndromic Hearing Loss in North African Moroccan Families.

Journal: Biomolecules

Published: March 03, 2026

CDH23-associated Usher syndrome: genotype-phenotype correlations.

Journal: Ophthalmic genetics

Published: February 19, 2026

Clinical Details of Low-Frequency Hearing Loss Observed in Autosomal Dominant MYO7A-Associated Hearing Loss Patients.

Journal: Genes

Published: February 13, 2026

Overlapping expression and co-operative function of the zebrafish pcdh15 paralogs.

Journal: Communications biology

Published: February 04, 2026

SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME.

Journal: American journal of ophthalmology

Published: January 21, 2026

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1-Related Autosomal Recessive Disorder Associated With Usher-Like Symptoms.

Journal: American journal of medical genetics. Part A

Published: January 02, 2026

Usher Syndrome Latest Advances

Find the Latest Research About Usher Syndrome

Mouse models and translational research progress of hereditary vestibular dysfunction.

Mouse models and translational research progress of hereditary vestibular dysfunction.

A regulatory axis for tonotopic MYO7A expression in cochlear hair cells.

A regulatory axis for tonotopic MYO7A expression in cochlear hair cells.

Identification of a recessive PCDH15 nonsense variant in purebred goats with vestibular dysfunction.

Identification of a recessive PCDH15 nonsense variant in purebred goats with vestibular dysfunction.

Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population-Specific Variants and Clinical Correlations.

Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population-Specific Variants and Clinical Correlations.

Somatic mosaicism of a novel USH2A variant in Usher syndrome.

Somatic mosaicism of a novel USH2A variant in Usher syndrome.

Heimler Syndrome Caused by Novel PEX6 Variants: Clinical and Genetic Characterization in a Saudi Cohort.

Heimler Syndrome Caused by Novel PEX6 Variants: Clinical and Genetic Characterization in a Saudi Cohort.

Molecular Characterization of Syndromic Hearing Loss in North African Moroccan Families.

Molecular Characterization of Syndromic Hearing Loss in North African Moroccan Families.

CDH23-associated Usher syndrome: genotype-phenotype correlations.

CDH23-associated Usher syndrome: genotype-phenotype correlations.

Clinical Details of Low-Frequency Hearing Loss Observed in Autosomal Dominant MYO7A-Associated Hearing Loss Patients.

Clinical Details of Low-Frequency Hearing Loss Observed in Autosomal Dominant MYO7A-Associated Hearing Loss Patients.

Overlapping expression and co-operative function of the zebrafish pcdh15 paralogs.

Overlapping expression and co-operative function of the zebrafish pcdh15 paralogs.

SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME.

SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME.

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1-Related Autosomal Recessive Disorder Associated With Usher-Like Symptoms.

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1-Related Autosomal Recessive Disorder Associated With Usher-Like Symptoms.