t/gene-dld

DLD gene

Discuss publications and research concerning the DLD gene.

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Related literature

Novel Biallelic Variants in DLD Gene Cause a Reversible Sensory Neuropathy.
DLD
Mutations within the predicted fragment-binding region of FAM83G/SACK1G abolish its interaction with the Ser/Thr kinase CK1α.
DLD
Deep Mutational Scanning of FDX1 Identifies Key Structural Determinants of Lipoylation and Cuproptosis.
DLD
Cellular Identification of Single-Base Mutations in KRAS Gene Fragments Based on Nonhomologous Spectroscopic Data Fusion Modeling.
DLD
Mutations within the predicted fragment-binding region of FAM83G/SACK1G abolish its interaction with the Ser/Thr kinase CK1α
DLD
Developmental language disorder - heritability and genetic correlations with other disorders affecting language.
DLD
Mendelian Randomization Study Reveals a Predicted Relationship between Sensorineural Hearing Loss and Mitochondrial Proteins.
DLD
Human iPSC-derived cerebral organoids model features of Leigh syndrome and reveal abnormal corticogenesis.
DLD
Enrichment of rare copy number variation in children with developmental language disorder.
DLD
Clinical characteristics and mutation analysis of five Chinese patients with maple syrup urine disease.
DLD

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