Lipoamide dehydrogenase deficiency in Ashkenazi Jews: an insertion mutation in the mitochondrial leader sequence

Prevalence of TB-related symptoms and self-reported disability among adult TB survivors.

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Single-Cell Transcriptomic Analysis of Kaposi Sarcoma.

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Fingernail form as a post-extraction guide for selecting the maxillary central incisor tooth form in the Saudi Arabian population: A novel application of CAD software.

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Xeroderma Pigmentosum Monozygotic Twins: Same Mutation Divergent Clinical Outcomes.

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X;7 Translocation at p21.1 and q31.31 Disrupting DMD: A Multiomics Study of a Male Dystrophinopathy Case.

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A Regulator SNP Affecting the Transcription Factor SP1 Binding Site in the PIK3R3 Gene Contributes to Noise-Induced Hearing Loss Risk.

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Functional Characterization and Genotype-Phenotype Correlation of Androgen Receptor Variants in Patients With Androgen Insensitivity Syndrome.

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Genotype-Phenotype Correlations and Their Implications for Personalized Genetic Counseling in 103 Patients With PRRT2 Mutations.

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Real-Time Monitoring with a Wristwatch-Type Sodium- and Potassium-Ion Sensor Using a Screen-Printed Liquid-Junction Reference Electrode.

ACS omega·2026

Anion-Dipole Catalytic Decomposition Enables Robust Solid Electrolyte Interfaces for Ah-Level Aqueous Zinc Batteries.

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Ion Channel Nano-Diagnostics for ER+ Breast Cancer.

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Crystallographically aligned Wadsley-Roth phase anodes with conductive agents for high-rate lithium-ion batteries.

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Hybrid machine learning framework for electrical grid stability prediction using comparative model evaluation.

Frontiers in artificial intelligence·2026

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Lipoamide dehydrogenase deficiency in Ashkenazi Jews: an insertion mutation in the mitochondrial leader sequence

Related Concept Videos

Prevalence of TB-related symptoms and self-reported disability among adult TB survivors.

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Standardized approach to extract candidate outcomes from literature for a standard outcome set: a case- and simulation study.

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Lipoamide dehydrogenase deficiency in Ashkenazi Jews: an insertion mutation in the mitochondrial leader sequence

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