Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2 (Q24651113)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2 |
scientific article |
Statements
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2 (English)
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January 2010
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86
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1
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65-71
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