[PDF] advancedotology.org

[PDF][PDF] Functional Analysis of Pendrin (SLC26A4) and its Pathogenic Mutations in cos-7 cells

H Zhanga, Y Feng, K Xia, L Jiang… - The Journal of …, 2012 - advancedotology.org
Objective: To investigate the mechanism of the deafness-causing mutation S448X in the
pendrin protein through measurement of the expression levels and functional activities of the …
被引用次数：1 相关文章

Functional Analysis of Pendrin (SLC26A4) and its Pathogenic Mutations in cos-7 cells

H Zhanga, Y Feng, K Xia, L Jiang… - The Journal of …, 2012 - search.proquest.com
Objective: To investigate the mechanism of the deafness-causing mutation S448X in the
pendrin protein through measurement of the expression levels and functional activities of the …

Functional Analysis of Pendrin (SLC26A4) and its Pathogenic Mutations in cos-7 cells.

H Zhanga, Y Feng, K Xia, L Jiang… - Journal of …, 2012 - search.ebscohost.com
Objective: To investigate the mechanism of the deafness-causing mutation S448X in the
pendrin protein through measurement of the expression levels and functional activities of the …
[PDF] advancedotology.org

[PDF][PDF] Functional Analysis of Pendrin (SLC26A4) and its Pathogenic Mutations in cos-7 cells

H Zhanga, Y Feng, K Xia, L Jiang, C He, L Mei - 2005 - advancedotology.org
Objective: To investigate the mechanism of the deafness-causing mutation S448X in the
pendrin protein through measurement of the expression levels and functional activities of the …
[PDF] archive.org

[PDF][PDF] Functional Analysis of Pendrin (SLC26A4) and its Pathogenic Mutations in cos-7 cells

H Zhanga, Y Feng, K Xia, L Jiang, C He, L Mei - 2005 - scholar.archive.org
Objective: To investigate the mechanism of the deafness-causing mutation S448X in the
pendrin protein through measurement of the expression levels and functional activities of the …

Functional Analysis of Pendrin (SLC26A4) and its Pathogenic Mutations in cos-7 cells.

H Zhanga, Y Feng, K Xia, L Jiang… - Journal of …, 2012 - search.ebscohost.com
Objective: To investigate the mechanism of the deafness-causing mutation S448X in the
pendrin protein through measurement of the expression levels and functional activities of the …