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GNPTAB-mucolipidosis
An autosomal recessive mucolipidosis disorder caused by bi-allelic variants in the GNPTAB gene. Symptoms of this condition occur across a clinical spectrum including mucolipidosis type II (ML II) and mucolipidosis type III alpha/beta (ML IIIα/β), and phenotypes intermediate between ML II and ML IIIα/β.
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Mucolipidosis type II 0 trials
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Mucolipidosis type III, alpha/beta 0 trials