A novel mutation of CLN3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
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3. The neuronal ceroid-lipofuscinoses (Batten disease): a new class of lysosomal storage diseases;Bennett;J. Inherit. Metab. Dis.,1999
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