Publication | Closed Access

Loss of Cytoplasmic Retention Ability of Mutant LKB1 Found in Peutz-Jeghers Syndrome Patients

Cytoplasmic Retention AbilityMendelian DisorderGenetic DisorderPeutz-jeghers Syndrome PatientsInherited Metabolic DiseasePathologyMutant Lkb1 FoundDisease Gene IdentificationMedicineCell BiologyCell SignalingLysosomal Storage Disease