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pro vyhledávání: '"Marte H. Hammersland"'
Publikováno v:
BMC Health Services Research, Vol 19, Iss 1, Pp 1-9 (2019)
Abstract Background Acute intermittent porphyria (AIP) is an inherited metabolic disease with low clinical penetrance caused by mutations in the hydroxymethylbilane (HMBS) gene. Although most patients experience little or no symptoms, serious attacks
Externí odkaz:
https://doaj.org/article/869bcafd787344258b9f31133e6cb868
Publikováno v:
BMC Health Services Research, Vol 19, Iss 1, Pp 1-9 (2019)
BMC Health Services Research
BMC Health Services Research
Background Acute intermittent porphyria (AIP) is an inherited metabolic disease with low clinical penetrance caused by mutations in the hydroxymethylbilane (HMBS) gene. Although most patients experience little or no symptoms, serious attacks may incl