Loss of LKB1 Kinase Activity in Peutz-Jeghers Syndrome, and Evidence for Allelic and Locus Heterogeneity - Concepedia

Concepedia

Publication | Open Access

Loss of LKB1 Kinase Activity in Peutz-Jeghers Syndrome, and Evidence for Allelic and Locus Heterogeneity

DOI Full Paper Access

215

Citations

29

References

1998

Year

Hamid Mehenni, Corinne Gehrig, Jun‐ichi Nezu, Asuka Oku, Miyuki Shimane, Colette Rossier, Nicolas Guex, Jean‐Louis Blouin, Hamish S. Scott, Stylianos E. Antonarakis

The American Journal of Human Genetics

Lkb1 Kinase ActivitySignal TransductionMendelian DisorderGenetic DisorderReceptor Tyrosine KinaseGeneticsInherited Metabolic DiseaseLocus HeterogeneityPeutz-jeghers SyndromeDisease Gene IdentificationMedicineCell BiologyCell SignalingCell Development

References

	Year	Citations

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