Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly
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| Description | scientific article published on 5 June 2008 |
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author: Maximilian Muenke Felicitas Lacbawan Jorge I Velez Jeffrey A Towbin John W. Belmont Elizabeth Goldmuntz Benjamin Feldman |
| Publication date | June 5, 2008 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |