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HGV.2016.2
HGV.2016.2
http://dx.doi.org/10.1038/HGV.2016.2
Characterization of the STK11 splicing variant as a normal splicing isomer in a patient with Peutz-Jeghers syndrome harboring genomic deletion of the STK11 gene
P356
Q36644008-AA99A6EE-E40C-47F4-8B92-BD7FA678BC9A
P356
HGV.2016.2
http://dx.doi.org/10.1038/HGV.2016.2