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Publications by Chin-Chu Tsai
Mutations of Cx26 Gene (GJB2) for Prelingual Deafness in Taiwan
European Journal of Human Genetics
Genetics
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Prevalence of Cx26 (GJB2) Gene Mutations Causing Recessive Nonsyndromic Hearing Impairment in India
International Journal of Human Genetics
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Recurrent Mutations in the Deafness Gene GJB2 (Connexin 26) in British Asian Families
Journal of Medical Genetics
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Cx26 Keratitis Ichthyosis Deafness Syndrome Mutations Trigger Alternative Splicing of Cx26 to Prevent Expression and Cause Toxicity in Vitro
Royal Society Open Science
Multidisciplinary
Mutations of Connexin 26 (GJB2) Gene in a Chinese Keratitis-Ichthyosis-Deafness Syndrome Patient With Squamous Cell Carcinoma
Journal of Dermatology
Dermatology
Medicine
Rapid Detection of the 35delG Mutation in the GJB2 Gene in Childhood Deafness
Journal of Medical Screening
Health Policy
Public Health
Occupational Health
Environmental
Connexin 26 (GJB2) Gene-Related Deafness and Speech Intelligibility After Cochlear Implantation
Otology and Neurotology
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Otorhinolaryngology
Sensory Systems
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A Novel Missense Mutation p.L76P in the GJB2 Gene Causing Nonsyndromic Recessive Deafness in a Brazilian Family
Brazilian Journal of Medical and Biological Research
Immunology
Cell Biology
Pharmacology
Biochemistry
Biophysics
Neuroscience
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Toxicology
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Pharmaceutics
Gene Therapy for Deafness
Gene Therapy
Molecular Medicine
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Molecular Biology
GJB2 ‐related Hearing Loss in Central Iran: Review of the Spectrum and Frequency of Gene Mutations
Annals of Human Genetics
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