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CLRN1
Cellular and Molecular Signatures in the Disease Tissue of Early
Supplementary Materials
Genome-Wide Association Study Identifies 44 Independent Genomic Loci for Self-Reported Adult Hearing Difficulty in the UK Biobank Cohort
Investigating the Effect of Chronic Activation of AMP-Activated Protein
Next Generation Sequencing Identifies Five Novel Mutations In
Retinal Disease in Usher Syndrome III Caused by Mutations in the Clarin-1 Gene
Predict AID Targeting in Non-Ig Genes Multiple Transcription Factor
Biallelic Mutation of CLRN2 Causes Non-Syndromic Hearing Loss in Humans
Analyzing the Mirna-Gene Networks to Mine the Important Mirnas Under Skin of Human and Mouse
Partial USH2A Deletions Contribute to Usher Syndrome in Denmark
Determining the Causes of Recessive Retinal Dystrophy
SACGHS Report on Gene Patents And
Two Novel Disease-Causing Mutations in the CLRN1 Gene in Patients with Usher Syndrome Type 3
Four-Year Follow-Up of Diagnostic Service in USH1 Patients
ABSTRACT Using a Bioinformatics Approach to Identify Genes That
Development and Application of a Next-Generation- Sequencing (NGS
A Big Data Perspective on the Genomics of Hearing Loss
Usher Syndrome
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Improving Hearing Loss Gene Testing: a Systematic Review of Gene Evidence Toward More Efficient Next-Generation Sequencing–Based Diagnostic Testing and Interpretation
Prognosticating Retinal Dystrophies in the Postgenomic Era Inheritance Patterns of Retinal Diseases
The Mechanosensory Structure of the Hair Cell Requires Clarin-1, a Protein Encoded by Usher Syndrome III Causative Gene
CLRN1 Gene Clarin 1
Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy
A Biallelic Variant in CLRN2 Causes Non-Syndromic Hearing Loss In
A Deep Intronic CLRN1 (USH3A) Founder Mutation Generates An
Genetics of Peripheral Vestibular Dysfunction: Lessons from Mutant Mouse Strains Sherri M