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t/gene-ucn

UCN gene

Discuss publications and research concerning the UCN gene.

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Related literature

Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant.
UCN
Two novel mitochondrial tRNA mutations, A7495G (tRNASer(UCN)) and C5577T (tRNATrp), are associated with seizures and cardiac dysfunction.
UCN
Splicing Defect in Mitochondrial Seryl-tRNA Synthetase Gene Causes Progressive Spastic Paresis Instead of HUPRA Syndrome.
UCN
Mitochondrial transfer RNA mutations and hypertension.
UCN
[Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss].
UCN
Analysis of serine codon conservation reveals diverse phenotypic constraints on hepatitis C virus glycoprotein evolution.
UCN
Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation.
UCN
Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.
UCN
Nonsyndromic hearing loss caused by a mitochondrial T7511C mutation.
UCN
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.
UCN

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