1. Windels, Mei-Lan, Cordier, Fleur, Van Dorpe, Jo, Ferdinande, Liesbeth, Creytens, David. 2024. PHOX2B: a diagnostic cornerstone in neurocristopathies and neuroblastomas. In Journal of clinical pathology, 77, 378-382. doi:10.1136/jcp-2023-209047. https://pubmed.ncbi.nlm.nih.gov/38458747/
2. Tyagi, Ankita, Goyal, Abhishek, Chaware, Prashant, Rathinam, Bertha A D. 2021. Mutations of PHOX2B Gene in Patients of Obesity Hypoventilation Syndrome in Central India. In Journal of laboratory physicians, 14, 164-168. doi:10.1055/s-0041-1735582. https://pubmed.ncbi.nlm.nih.gov/35982870/
3. Trang, Ha, Samuels, Martin, Ceccherini, Isabella, Porto-Abal, Raquel, Katz-Salamon, Miriam. 2020. Guidelines for diagnosis and management of congenital central hypoventilation syndrome. In Orphanet journal of rare diseases, 15, 252. doi:10.1186/s13023-020-01460-2. https://pubmed.ncbi.nlm.nih.gov/32958024/
4. Zhou, Amy, Rand, Casey M, Hockney, Sara M, Yap, Kai Lee, Weese-Mayer, Debra E. 2021. Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype-phenotype correlation in congenital central hypoventilation syndrome (CCHS). In Genetics in medicine : official journal of the American College of Medical Genetics, 23, 1656-1663. doi:10.1038/s41436-021-01178-x. https://pubmed.ncbi.nlm.nih.gov/33958749/
5. Lin, Ao, Fu, Wen, Wang, Wenwen, Liu, Guochang, He, Jing. . Association between PHOX2B gene rs28647582 T>C polymorphism and Wilms tumor susceptibility. In Bioscience reports, 39, . doi:10.1042/BSR20192529. https://pubmed.ncbi.nlm.nih.gov/31652452/
6. Bourdeaut, Franck, Trochet, Delphine, Janoueix-Lerosey, Isabelle, Amiel, Jeanne, Delattre, Olivier. . Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma. In Cancer letters, 228, 51-8. doi:. https://pubmed.ncbi.nlm.nih.gov/15949893/
7. Bachetti, Tiziana, Ceccherini, Isabella. 2019. Causative and common PHOX2B variants define a broad phenotypic spectrum. In Clinical genetics, 97, 103-113. doi:10.1111/cge.13633. https://pubmed.ncbi.nlm.nih.gov/31444792/
8. Crawford, Mark W. 2011. The paired-like homeobox 2B (PHOX2B) gene and respiratory control. In Canadian journal of anaesthesia = Journal canadien d'anesthesie, 58, 1063-8. doi:10.1007/s12630-011-9591-6. https://pubmed.ncbi.nlm.nih.gov/22006076/
9. Marion, Tara L, Bradshaw, Wanda T. . Congenital central hypoventilation syndrome and the PHOX2B gene mutation. In Neonatal network : NN, 30, 397-401. doi:10.1891/0730-0832.30.6.397. https://pubmed.ncbi.nlm.nih.gov/22052119/
10. Yarmarkovich, Mark, Marshall, Quinlen F, Warrington, John M, Kiefel, Ben R, Maris, John M. 2023. Targeting of intracellular oncoproteins with peptide-centric CARs. In Nature, 623, 820-827. doi:10.1038/s41586-023-06706-0. https://pubmed.ncbi.nlm.nih.gov/37938771/