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Mild Persistent Isolated Hypermethioninemia Identified through Newborn Screening in Michigan.
Sen, Kuntal; Felice, Michael D; Bannick, Allison; Colombo, Roberto; Conway, Robert L.
Affiliation
  • Sen K; Division of Genetic, Genomic and Metabolic Disorders, Children's Hospital of Michigan, Detroit, Michigan, United States.
  • Felice MD; Wayne State University School of Medicine, Detroit, Michigan, United States.
  • Bannick A; Wayne State University School of Medicine, Detroit, Michigan, United States.
  • Colombo R; Division of Genetic, Genomic and Metabolic Disorders, Children's Hospital of Michigan, Detroit, Michigan, United States.
  • Conway RL; Center for the Study of Rare Inherited Diseases (CeSMER), Niguarda Ca' Granda Metropolitan Hospital, Milan, Italy.
J Pediatr Genet ; 8(2): 54-57, 2019 Jun.
Article in En | MEDLINE | ID: mdl-31061746
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Screening_studies Language: En Journal: J Pediatr Genet Year: 2019 Type: Article Affiliation country: United States
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Screening_studies Language: En Journal: J Pediatr Genet Year: 2019 Type: Article Affiliation country: United States