(Q50495597)
Statements
Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family. (English)
1 reference
A L Wilgoss
1 reference
G Richard
1 reference
H P Stevens
1 reference
C S Munro
1 reference
I M Leigh
1 reference
1 June 2000
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8
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6
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469-472
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Identifiers
1 reference