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pro vyhledávání: '"Simona, Bagnasco"'
Autor:
Tiziana Bachetti, Simona Bagnasco, Raffaele Piumelli, Antonella Palmieri, Isabella Ceccherini
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Heterozygous mutations in the Paired like homeobox 2b (PHOX2B) gene are causative of congenital central hypoventilation syndrome (CCHS), a rare monogenic disorder belonging to the family of neurocristopathies and due to a defective development of the
Externí odkaz:
https://doaj.org/article/f51f4ed5839f4684936e72fcb9017c8a
Autor:
Tiziana, Bachetti, Simona, Bagnasco, Raffaele, Piumelli, Antonella, Palmieri, Isabella, Ceccherini
Publikováno v:
Frontiers in Neurology
Heterozygous mutations in the Paired like homeobox 2b (PHOX2B) gene are causative of congenital central hypoventilation syndrome (CCHS), a rare monogenic disorder belonging to the family of neurocristopathies and due to a defective development of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd68a132a1f3105fb7821e61c9e0edf9
https://pubmed.ncbi.nlm.nih.gov/33815256
https://pubmed.ncbi.nlm.nih.gov/33815256