NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway (Q24293498)
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Current Data About NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway
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(P1476) "NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway" (language: en)
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(P2093) Ryan McDaniell
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Daniel M Warthen
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Pedro A Sanchez-Lara
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Ian D Krantz
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David A Piccoli
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Nancy B Spinner
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