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Nonsyndromic arteriopathy and aortopathy and vascular Ehlers-Danlos syndrome causing COL3A1 variants.
Yagi, Hiroki; Takeda, Norifumi; Amiya, Eisuke; Akiyama, Nana; Chang, Hyangri; Ishiura, Hiroyuki; Sato, Jiro; Akazawa, Hiroshi; Morita, Hiroyuki; Komuro, Issei.
Affiliation
  • Yagi H; Department of Cardiovascular Medicine, The University of Tokyo Hospital, Tokyo, Japan.
  • Takeda N; Marfan Syndrome Center, The University of Tokyo Hospital, Tokyo, Japan.
  • Amiya E; Department of Cardiovascular Medicine, The University of Tokyo Hospital, Tokyo, Japan.
  • Akiyama N; Marfan Syndrome Center, The University of Tokyo Hospital, Tokyo, Japan.
  • Chang H; Department of Cardiovascular Medicine, The University of Tokyo Hospital, Tokyo, Japan.
  • Ishiura H; Marfan Syndrome Center, The University of Tokyo Hospital, Tokyo, Japan.
  • Sato J; Department of Genomic Medicine, The University of Tokyo Hospital, Tokyo, Japan.
  • Akazawa H; Marfan Syndrome Center, The University of Tokyo Hospital, Tokyo, Japan.
  • Morita H; Department of Genomic Medicine, The University of Tokyo Hospital, Tokyo, Japan.
  • Komuro I; Marfan Syndrome Center, The University of Tokyo Hospital, Tokyo, Japan.
Am J Med Genet A ; 188(9): 2777-2782, 2022 09.
Article in En | MEDLINE | ID: mdl-35543214
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ehlers-Danlos Syndrome Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2022 Document type: Article Affiliation country: Japan Country of publication: United States
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ehlers-Danlos Syndrome Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2022 Document type: Article Affiliation country: Japan Country of publication: United States