Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms.

L. Cremonesi, A. Cozzi, D. Girelli, F. Ferrari, I. Fermo, B. Foglieni, S. Levi, C. Bozzini, M. Camparini, M. Ferrari, P. Arosio

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
JournalJournal of Medical Genetics
Volume41
Issue number6
Publication statusPublished - Jun 2004

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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