Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

被引：48

作者：

Ben-Yosef, T

Wattenhofer, M

Riazuddin, S

Ahmed, ZM

Scot, HS

Kudoh, J

Shibuya, K

Antonarakis, SE

Bonne-Tamir, B

Radhakrishna, U

Naz, S

Ahmed, Z

Riazuddin, S

Pandya, A

Nance, WE

Wilcox, ER

Friedman, TB

Morell, RJ

机构：

[1] NIDCD, Genet Mol Lab, NIH, Rockville, MD 20850 USA

[2] Univ Geneva, Sch Med, Grad Program Mol & Cellular Biol, CH-1211 Geneva, Switzerland

[3] Univ Punjab, Ctr Excellence Mol Biol, Lahore, Pakistan

[4] Univ Geneva, Sch Med, Div Med Genet, CH-1211 Geneva, Switzerland

[5] Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan

[6] Tel Aviv Univ, Sackler Sch Med, Dept Human Genet & Mol Med, IL-69978 Tel Aviv, Israel

[7] Virginia Commonwealth Univ, Dept Human Genet, Richmond, VA 23298 USA

来源：

JOURNAL OF MEDICAL GENETICS | 2001年 / 38卷 / 06期

关键词：

D O I：

10.1136/jmg.38.6.396

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：396 / 400

页数：5

共 18 条

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