Citace podle APA

Gowda, V. K., Amoghimath, R., Srinivasan, V. M., & Bhat, M. (2017). Sandhoff Disease without Hepatosplenomegaly Due to Hexosaminidase B Gene Mutation. J Pediatr Neurosci.

Styl Chicago

Gowda, Vykuntaraju K., Raghavendraswami Amoghimath, Varun M. Srinivasan, a Maya Bhat. "Sandhoff Disease Without Hepatosplenomegaly Due to Hexosaminidase B Gene Mutation." J Pediatr Neurosci 2017.

Citace podle MLA

Gowda, Vykuntaraju K., Raghavendraswami Amoghimath, Varun M. Srinivasan, a Maya Bhat. "Sandhoff Disease Without Hepatosplenomegaly Due to Hexosaminidase B Gene Mutation." J Pediatr Neurosci 2017.

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