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Co-occurrence of the Poland sequence in a patient with the cobalamin C defect: more than just a coincidence?

AuthorsJames D Weisfeld-Adams, Peter R Baker
JournalJournal of inherited metabolic disease (J Inherit Metab Dis) Vol. 38 Issue 2 Pg. 365-6 (Mar 2015) ISSN: 1573-2665 [Electronic] United States
PMID25388550 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Carrier Proteins
  • MMACHC protein, human
  • Oxidoreductases
Topics
  • Carrier Proteins (genetics)
  • Genetic Predisposition to Disease
  • Homocystinuria (diagnosis, genetics)
  • Humans
  • Infant, Newborn
  • Male
  • Oxidoreductases
  • Phenotype
  • Poland Syndrome (diagnosis, genetics)
  • Sequence Deletion
  • Vitamin B 12 Deficiency (congenital, diagnosis, genetics)

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