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pro vyhledávání: '"Hydroxyacyl-coenzyme A dehydrogenase (HADH) gene"'
Autor:
Wei Zhang, Yan-Mei Sang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Abstract Congenital hyperinsulinism (CHI), a major cause of persistent and recurrent hypoglycemia in infancy and childhood. Numerous pathogenic genes have been associated with 14 known genetic subtypes of CHI. Adenosine triphosphate-sensitive potassi
Externí odkaz:
https://doaj.org/article/2908596c4be040aa945717fa264cffa3
Autor:
Yan-Mei Sang, Wei Zhang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Congenital hyperinsulinism (CHI), a major cause of persistent and recurrent hypoglycemia in infancy and childhood. Numerous pathogenic genes have been associated with 14 known genetic subtypes of CHI. Adenosine triphosphate-sensitive potassium channe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c2e6ebcd001236c75a4ec1efe7cf8c3
https://doaj.org/article/2908596c4be040aa945717fa264cffa3
https://doaj.org/article/2908596c4be040aa945717fa264cffa3
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