Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1

Additional information for mutational screening.

C. Asteria, G. Faglia, R. Roncoroni, G. Borretta, P. Ribotto, P. Beck-Peccoz

Research output: Contribution to journalArticle

8 Citations (Scopus)
Original languageEnglish
Pages (from-to)237
Number of pages1
JournalHuman Mutation
Volume17
Issue number3
Publication statusPublished - Mar 2001

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1 : Additional information for mutational screening. / Asteria, C.; Faglia, G.; Roncoroni, R.; Borretta, G.; Ribotto, P.; Beck-Peccoz, P.

In: Human Mutation, Vol. 17, No. 3, 03.2001, p. 237.

Research output: Contribution to journalArticle

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