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Paper Details

A mosaic PTEN mutation causing Cowden syndrome identified by deep sequencing.
Genet Med
22
2013
768delAG, Cowden syndrome, Lhermitte-Duclos disease, PTEN, PTEN gene, PTEN locus, PTEN mutation, PTEN mutations, blood leukocytes, c.767, c.767_768delAG, cerebellar tumor, skin fibroblasts, woman
Author NameAffiliation
Colin C PritchardUniversity of Washington
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