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Q33577799-94DE161D-E933-4C4D-ACF7-1B0E68A2D690
Q33577799-94DE161D-E933-4C4D-ACF7-1B0E68A2D690
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33577799-94DE161D-E933-4C4D-ACF7-1B0E68A2D690
Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome
P2860
Q33577799-94DE161D-E933-4C4D-ACF7-1B0E68A2D690
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33577799-94DE161D-E933-4C4D-ACF7-1B0E68A2D690
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wasDerivedFrom
445c613fa15161b719b2a5df96469c6b7d3682ea
P2860
Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome