Two Italian patients with novel AAAS gene mutation expand allelic and phenotypic spectrum of triple A (Allgrove) syndrome

C. Palka, R. Giuliani, F. Brancati, A. Mohn, A. Di Muzio, O. Calabrese, A. Huebner, D. De Grandis, F. Chiarelli, A. Ferlini, L. Stuppia

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)298-301
Number of pages4
JournalClinical Genetics
Issue number3
Publication statusPublished - Mar 2010

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

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