Déficit de 3-hidroxiacil-CoA-deshidrogenasa de cadena larga: a propósito de un caso
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference10 articles.
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1. Retinitis pigmentosa as a clinical presentation of LCHAD deficiency: A clinical case and review of the literature;Archivos de la Sociedad Española de Oftalmología (English Edition);2021-09
2. Retinosis pigmentaria como clínica de presentación del déficit de LCHAD: caso clínico y revisión de la literatura;Archivos de la Sociedad Española de Oftalmología;2021-09
3. Expanding the genotype–phenotype correlation of childhood sensory polyneuropathy of genetic origin;Scientific Reports;2020-09-30
4. Diagnosis and treatment of the long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHAD) in a 8 months old infant;Russian Pediatric Journal;2020-08-06
5. Follow-up and multimodal imaging in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency;International Journal of Ophthalmology;2018-10-18
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