Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82. (Q33960515)
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Current Data About Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.
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(P1932) Mary-Claire King

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(P1932) Moien Kanaan
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(P1932) Tom Walsh
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(P1932) Karen B Avraham
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(P1476) "Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82." (language: en)
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(P2093) Hashem Shahin
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Tal Elkan-Miller
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Ming K Lee
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Anne M Thornton
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Wendy Roeb
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Amal Abu Rayyan
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Suheir Loulus
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External Links
(P356) 10.1016/J.AJHG.2010.05.010
(P698) 20602914
(P932) 2896776
(P5875) 45093954