Mechanism of Two Novel Human GJC3 Missense Mutations in Causing Non-Syndromic Hearing Loss

Human Connexin30.2/31.3 (GJC3) does not Form Functional Gap Junction Channels but Causes Enhanced ATP Release in HeLa Cells

(2011) Wei-Guang Liang et al.   CELL BIOCHEMISTRY AND BIOPHYSICS

Structural and functional studies of gap junction channels

(2010) So Nakagawa et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation

(2010) Jiann-Jou Yang et al.   HUMAN GENETICS

Asymmetric Configurations and N-terminal Rearrangements in Connexin26 Gap Junction Channels

(2010) Atsunori Oshima et al.   JOURNAL OF MOLECULAR BIOLOGY

Identification of Novel Variants in the Cx29 Gene of Nonsyndromic Hearing Loss Patients Using Buccal Cells and Restriction Fragment Length Polymorphism Method

(2009) Wen-Hung Wang et al.   AUDIOLOGY AND NEURO-OTOLOGY

A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss

(2009) Hui-Mei Hong et al.   HUMAN GENETICS

Structure of the connexin 26 gap junction channel at 3.5 Å resolution

(2009) Shoji Maeda et al.   NATURE