The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes (Q28585278)
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scientific journal article
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English | The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes |
scientific journal article |
Statements
D. Duboule
S. Bruneau
K. R. Johnson
M. Yamamoto