Publication | Closed Access
A novel X–linked gene, DDP, shows mutations in families with deafness (DFN–1), dystonia, mental deficiency and blindness
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Citations
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References
1996
Year
Neurodevelopmental DisordersGenetic DiseasesDevelopmental BiologyMendelian DisorderMental DeficiencyGenetic DisorderGeneticsFragile X SpectrumNeurogeneticsMolecular GeneticsMedical GeneticsDisease Gene IdentificationGenetic BasisMedicineFragile X PremutationMonogenic Disorders
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