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Juvenile Tay Sachs Disease Due to Compound Heterozygous Mutation in Hex-A Gene, with Early Sign of Bilateral Tremors

Detalles Bibliográficos
Autores principales:	Sheth, Jayesh, Mohapatra, Ira, Patra, Gangotri, Bhavsar, Riddhi, Patel, Chandni, Shah, Siddharth, Nair, Aadhira
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350779/ https://www.ncbi.nlm.nih.gov/pubmed/35936646 http://dx.doi.org/10.4103/aian.aian_577_21

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