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pro vyhledávání: '"Ibrahim Al Sbou"'
Autor:
Raida Khalil, Eman Albsoul, Nesrin Mwafi, Arwa Alsaraireh, Ibrahim Al Sbou, Dema Ali, Loiy Obeidat
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2021 (2021)
BioMed Research International, Vol 2021 (2021)
Background. Metabolic disorder alkaptonuria is an autosomal recessive disorder caused by mutations in the HGD gene, and a deficiency HGD enzyme activity results in an accumulation of homogentisic acid (HGA), ochronosis, and destruction of connective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cadfc0daeb13efef0113a7ce92af64fd
