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pro vyhledávání: '"H.S. Meghavathi"'
Publikováno v:
Global Medical Genetics, Vol 10, Iss 02, Pp 105-108 (2023)
Congenital disorder of glycosylation (CDG) is an autosomal recessively inherited disorder. Hypotonia, stroke-like episodes, and peripheral neuropathy are also associated with the condition that typically develops during infancy. The patient, a 12-yea
Externí odkaz:
https://doaj.org/article/2b66589928614bfc8e5ed01baa054e8d