关键词: Abetalipoproteinaemia MTTP gene central hypothyroidism novel mutation
Mesh : Abetalipoproteinemia / complications genetics pathology Carrier Proteins / genetics Female Humans Hypothyroidism / complications genetics pathology Infant Mutation Prognosis
来 源:
DOI:10.4274/jcrpe.galenos.2019.2019.0144
PDF(Pubmed)