Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome
| Data(s) |
17/03/2005
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| Resumo |
Background: Germline mutations or large-scale deletions in the coding region and splice sites of STK11/LKB1 do not account for all cases of Peutz-Jeghers syndrome (PJS). It is conceivable that, on the basis of data from other diseases, inherited variation in promoter elements of STK11/LKB1 may cause PJS. |
| Identificador | |
| Idioma(s) |
eng |
| Direitos |
info:eu-repo/semantics/restrictedAccess |
| Fonte |
Hearle , N C M , Tomlinson , I , Lim , W , Murday , V , Swarbrick , E , Lim , G , Phillips , R , Lee , P , O'Donohue , J , Trembath , R C , Morrison , P , Norman , A , Taylor , R , Hodgson , S , Lucassen , A & Houlston , R S 2005 , ' Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome ' BMC Genomics , vol 6 . DOI: 10.1186/1471-2164-6-38 |
| Palavras-Chave | #/dk/atira/pure/subjectarea/asjc/2700 #Medicine(all) |
| Tipo |
article |
