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pro vyhledávání: '"Pengjiang Kang"'
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Thiamine-responsive megaloblastic anemia syndrome (TRMA) is a rare autosomal recessive hereditary disease due to mutations in SLC19A2. Some cases show familial inheritance.Case report: A female patient (from a gravida 1, para 1 mother) of
Externí odkaz:
https://doaj.org/article/59850e3120964d1ea67f0dcd3ffcd3ab
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics
Frontiers in Pediatrics
Background: Thiamine-responsive megaloblastic anemia syndrome (TRMA) is a rare autosomal recessive hereditary disease due to mutations in SLC19A2. Some cases show familial inheritance.Case report: A female patient (from a gravida 1, para 1 mother) of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bc1eb812a323e7fdfd169297f24f985
https://doi.org/10.3389/fped.2021.630329
https://doi.org/10.3389/fped.2021.630329