Variable human phenotype associated with novel deletions of the PHOX2B gene
Year: 2011
Type: article
Study design: Observational Study
Source: Pediatric Pulmonology
DOI: 10.1002/ppul.21527
Language: English
Subfield: Endocrine and Autonomic Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W1964336355
