Your browser doesn't support javascript.
loading
Primary ovarian insufficiency in a female with phosphomannomutase-2 gene (PMM2) mutations for congenital disorder of glycosylation.
Masunaga, Yohei; Mochizuki, Mie; Kadoya, Machiko; Wada, Yoshinao; Okamoto, Nobuhiko; Fukami, Maki; Kato, Fumiko; Saitsu, Hirotomo; Ogata, Tsutomu.
Affiliation
  • Masunaga Y; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
  • Mochizuki M; Department of Pediatrics, University of Yamanashi, Faculty of Medicine, Chuou 409-3898, Japan.
  • Kadoya M; Department of Molecular Medicine, Osaka Women's and Children's Hospital, Izumi 594-1101, Japan.
  • Wada Y; Department of Molecular Medicine, Osaka Women's and Children's Hospital, Izumi 594-1101, Japan.
  • Okamoto N; Department of Molecular Medicine, Osaka Women's and Children's Hospital, Izumi 594-1101, Japan.
  • Fukami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan.
  • Kato F; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
  • Saitsu H; Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
  • Ogata T; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
Endocr J ; 68(5): 605-611, 2021 May 28.
Article in En | MEDLINE | ID: mdl-33583911
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Primary Ovarian Insufficiency / Phosphotransferases (Phosphomutases) / Congenital Disorders of Glycosylation Type of study: Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Endocr J Journal subject: ENDOCRINOLOGIA Year: 2021 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Primary Ovarian Insufficiency / Phosphotransferases (Phosphomutases) / Congenital Disorders of Glycosylation Type of study: Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Endocr J Journal subject: ENDOCRINOLOGIA Year: 2021 Document type: Article Affiliation country: Country of publication: