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
Year: 2003
Type: article
DOI: 10.1086/346092
Institutions: KU Leuven, The University of Osaka
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Award: G4493082561
OpenAlex ID: W2164448409
