Unusual Splice-Site Mutations in the RSK2 Gene and Suggestion of Genetic Heterogeneity in Coffin-Lowry Syndrome - Concepedia

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Unusual Splice-Site Mutations in the RSK2 Gene and Suggestion of Genetic Heterogeneity in Coffin-Lowry Syndrome

DOI Full Paper Access

37

Citations

22

References

2002

Year

Maria Zeniou, Solange Pannetier, Jean‐Pierre Fryns, André Hanauer

The American Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseUnusual Splice-site MutationsPathologyMolecular GeneticsDisease Gene IdentificationMedicineCoffin-lowry SyndromeRsk2 Gene

References

	Year	Citations

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