(Q50491548)
Statements
Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population. (English)
1 reference
H Gabriel
1 reference
P Kupsch
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J Sudendey
1 reference
E Winterhager
1 reference
K Jahnke
1 reference
J Lautermann
1 reference
1 June 2001
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17
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6
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521-522
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Identifiers
1 reference