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Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations.

AuthorsP M Dahia, O Gimm, H Chi, D J Marsh, P R Reynolds, C Eng
JournalJournal of medical genetics (J Med Genet) Vol. 37 Issue 9 Pg. 715-7 (Sep 2000) ISSN: 1468-6244 [Electronic] England
PMID11182934 (Publication Type: Letter, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Tumor Suppressor Proteins
  • DNA
  • Phosphoric Monoester Hydrolases
  • multiple inositol-polyphosphate phosphatase
  • PTEN Phosphohydrolase
  • PTEN protein, human
Topics
  • Centromere
  • DNA (chemistry, genetics)
  • DNA Mutational Analysis
  • Germ-Line Mutation
  • Hamartoma Syndrome, Multiple (genetics, pathology)
  • Humans
  • PTEN Phosphohydrolase
  • Phosphoric Monoester Hydrolases (genetics)
  • Syndrome
  • Tumor Suppressor Proteins

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