Germline Mosaicism Of PHOX2B Mutation Accounts For Familial Recurrence Of Congenital Central Hypoventilation Syndrome (CCHS)
Year: 2012
Type: conference-abstract
Language: English
Subfield: Endocrine and Autonomic Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2327710072
