(PDF) Identification of CDH23 Mutations in Korean Families

Identification of CDH23 Mutations in Korean Families With Hearing Loss by Whole-Exome Sequencing

BMC Medical Genetics - United Kingdom

doi 10.1186/1471-2350-15-46

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April 28, 2014

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Springer Science and Business Media LLC

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Identification of CDH23 Mutations in Korean Families With Hearing Loss by Whole-Exome Sequencing

BMC Medical Genetics - United Kingdom

doi 10.1186/1471-2350-15-46

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing

Identification of Novel EXT Mutations in Patients With Hereditary Multiple Exostoses Using Whole-Exome Sequencing

Whole-Exome Sequencing Identifies Causative Mutations in Families With Congenital Anomalies of the Kidney and Urinary Tract

TCOF1 Pathogenic Variants Identified by Whole-Exome Sequencing in Chinese Treacher Collins Syndrome Families and Hearing Rehabilitation Effect

Family-Based Whole-Exome Sequencing Identifies Novel Loss-Of-Function Mutations of FBN1 for Marfan Syndrome

Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families

Novel Mutations in SPTA1 and SPTB Identified by Whole Exome Sequencing in Eight Thai Families With Hereditary Pyropoikilocytosis Presenting With Severe Fetal and Neonatal Anaemia

Whole-Exome Sequencing Identifies Somatic ATRX Mutations in Pheochromocytomas and Paragangliomas

Whole Exome Sequencing in Extended Families With Autism Spectrum Disorder Implicates Four Candidate Genes