A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss.
Hong, Hui-Mei
A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss. [electronic resource] - Human genetics Feb 2010 - 191-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1432-1203
10.1007/s00439-009-0758-y doi
Cell Membrane--metabolism
Cell Survival
Connexins--chemistry
Endoplasmic Reticulum--metabolism
Gap Junctions--metabolism
Green Fluorescent Proteins--genetics
HeLa Cells
Hearing Loss--genetics
Humans
Microscopy, Fluorescence
Mutant Proteins--chemistry
Mutation, Missense
Nerve Tissue Proteins--chemistry
Protein Multimerization
Recombinant Fusion Proteins--genetics
Transfection
A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss. [electronic resource] - Human genetics Feb 2010 - 191-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1432-1203
10.1007/s00439-009-0758-y doi
Cell Membrane--metabolism
Cell Survival
Connexins--chemistry
Endoplasmic Reticulum--metabolism
Gap Junctions--metabolism
Green Fluorescent Proteins--genetics
HeLa Cells
Hearing Loss--genetics
Humans
Microscopy, Fluorescence
Mutant Proteins--chemistry
Mutation, Missense
Nerve Tissue Proteins--chemistry
Protein Multimerization
Recombinant Fusion Proteins--genetics
Transfection