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pro vyhledávání: '"Jingxiang Han"'
Publikováno v:
Stem Cell Research, Vol 60, Iss , Pp 102695- (2022)
Prader–Willi syndrome (PWS) is a neurodevelopmental disorder caused by deficiency of paternal gene expression in the 15q11.2-q13 chromosome imprinted region. Hyperphagia and dysgnosia are typical clinical features in the early-childhood of patient.
Externí odkaz:
https://doaj.org/article/94e11b24523e4af98cf3f9165f1d35ef