Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1 - Concepedia

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Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1

DOI Full Paper Access

24

Citations

13

References

2011

Year

Lars R. Jensen, Wei Chen, Bettina A. Moser, Bettina Lipkowitz, Christopher Schroeder, Luciana Musante, Andreas Tzschach, Vera M. Kalscheuer, Ilaria Meloni, Martine Raynaud,

European Journal of Human Genetics

Somatic VariantGenetic DisorderGeneticsFragile X SpectrumMolecular BiologyHybridisation-based ResequencingMolecular GeneticsDisease Gene IdentificationMedicine

References

	Year	Citations

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