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Early Infantile Leigh-like SLC19A3 Gene Defects Have a Poor Prognosis: Report and Review

Solute carrier family 19 (thiamine transporter), member 3 (SCL19A3) gene defect produces an autosomal recessive neurodegenerative disorder associated with different phenotypes and acronyms. One of the common presentations is early infantile lethal Leigh-like syndrome. We report a case of early infan...

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Detalles Bibliográficos
Autor principal:	Alfadhel, Majid
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661663/ https://www.ncbi.nlm.nih.gov/pubmed/29123435 http://dx.doi.org/10.1177/1179573517737521

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