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Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect: Infantile presentation of Batten's disease. J Child Neurology

De los Reyes E, Dyken PR, Phillips PH, Brodsky M, Bates S, Glasier C, Mrak R. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect: Infantile presentation of Batten's disease. J Child Neurology. 2004; 19:42-46.


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