DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Gowda VK, Amoghimath R, Srinivasan VM, Bhat M.
Sandhoff disease without hepatosplenomegaly due to hexosaminidase B gene mutation.
J Pediatr Neurosci 2017;
12 (01) 78-79
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