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Summary Expression Phenotypes Gene Literature (5) GO Terms (6) Nucleotides (92) Proteins (36) Interactants (230) Wiki
XB--5762129

Papers associated with apcdd1 (and Disease Ontology)



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APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex., Shimomura Y, Agalliu D, Vonica A, Luria V, Wajid M, Baumer A, Belli S, Petukhova L, Schinzel A, Brivanlou AH, Brivanlou AH, Barres BA, Christiano AM., Nature. April 15, 2010; 464 (7291): 1043-7.      

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