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
Descripción
Sumario:

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