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Q50357721-B0B072DD-C2B3-41AC-B6CA-0775F4E4EF81
Q50357721-B0B072DD-C2B3-41AC-B6CA-0775F4E4EF81
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Statement
http://www.wikidata.org/entity/statement/Q50357721-B0B072DD-C2B3-41AC-B6CA-0775F4E4EF81
SLC26A4 mutation frequency and spectrum in 109 Danish Pendred syndrome/DFNB4 probands and a report of nine novel mutations.
P2860
Q50357721-B0B072DD-C2B3-41AC-B6CA-0775F4E4EF81
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50357721-B0B072DD-C2B3-41AC-B6CA-0775F4E4EF81
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Statement
wasDerivedFrom
ada0b710f93d7c16e5b7b13e9d683e21fa08ce21
P2860
Mutation analysis of SLC26A4 for Pendred syndrome and nonsyndromic hearing loss by high-resolution melting