Work

Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH

Year: 2011

Type: article

Study design: Observational Study

Source: Human Genetics

DOI: 10.1007/s00439-011-1078-6

Authors: Daniel E. Pineda-Alvarez, Erich Roessler, Ping Hu, Kshitij Srivastava, Benjamin D. Solomon, C. Evan Siple, Chen-Ming Fan, Maximilian Muenke

Institutions: National Institutes of Health, National Human Genome Research Institute, Carnegie Institution for Science, Department of Embryology

Language: English

Topic: Fetal and Pediatric Neurological Disorders

Subfield: Pediatrics, Perinatology and Child Health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: green

Funders: National Human Genome Research Institute, National Institute of Diabetes and Digestive and Kidney Diseases

Award: Formation of the Enteric Nervous System

OpenAlex ID: W1985484488

FWCI: 5.628

Cites: 40

Cited by: 57

Related to: 10