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GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985
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Related Tags
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cherry red spot
enzyme,defect
gangliosidosis GM1
genetic neurologic disorders
hepatosplenomegaly
hypotonia
inborn errors of metabolism
lipid storage disorder of CNS
macrocephaly
mortality
urine test for metabolic disorders
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