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  • A syndrome characterized by degenerative and proliferative changes of the neuroretina resulting in congenital blindness along with progressive mental disorders in about 50% of patients and sensorineural deafness in about 33% of patients, and that has_material_basis_in mutation in the NDP gene on chromosome Xp11.
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  • url:https://www.ncbi.nlm.nih.gov/pubmed/1303235
  • url:https://www.ncbi.nlm.nih.gov/pubmed/13998843
  • url:https://www.ncbi.nlm.nih.gov/pubmed/7627181
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