Zobrazeno 1 - 2
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pro vyhledávání: '"Ecem Narin"'
Publikováno v:
Journal of Contemporary Medicine, Vol 11, Iss 6, Pp 924-926 (2021)
Hereditary methemoglobinemia is one of the rare causes of hypoxemia. Mutations in the CYB5R3 gene cause autosomal recessive hereditary methemoglobinemia. Mostly, symptoms such as shortness of breath, bruise and and fatique occur. It may not display a
Externí odkaz:
https://doaj.org/article/d950ed03eebd430b93bc400eff116ca4
Publikováno v:
Journal of Contemporary Medicine, Vol 11, Iss 6 (Early Access-Erken Görünüm), Pp 0-0 (2021)
Hereditary methemoglobinemia is one of the rare causes of hypoxemia. Mutations in the CYB5R3 gene cause autosomal recessive hereditary methemoglobinemia. Mostly, symptoms such as shortness of breath, bruise and and fatique occur. It may not display a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7696afc3163687a3e52944e841b5eeb5
https://dergipark.org.tr/tr/pub/jcm/issue/64517/946473
https://dergipark.org.tr/tr/pub/jcm/issue/64517/946473