Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82. (Q33960515)
Jump to navigation
Jump to search
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82. |
scientific article |
Statements
1 reference
Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82. (English)
1 reference
Hashem Shahin
1 reference
Tal Elkan-Miller
1 reference
Ming K Lee
1 reference
Anne M Thornton
1 reference
Wendy Roeb
1 reference
Amal Abu Rayyan
1 reference
Suheir Loulus
1 reference
17 June 2010
1 reference
1 reference
87
1 reference
90-94
1 reference
Identifiers
1 reference
1 reference
1 reference