Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31 - Concepedia

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Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

DOI Full Paper Access

116

Citations

45

References

2008

Year

Xue-Zhong Liu, Yongyi Yuan, Denise Yan, Emilie Hong Ding, Xiao Mei Ouyang, Fei Yu, Wenxue Tang, Huijun Yuan, Qing Chang, Li Du,

Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsGap JunctionMolecular GeneticsNon-syndromic DeafnessMolecular NeurobiologyDisease Gene IdentificationMedicineDigenic Inheritance

References

	Year	Citations

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