Title : A novel cause for primordial dwarfism revealed: defective tRNA modification.

Pub. Date : 2015 Oct 1

PMID : 26429597






1 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 A mutation in the WDR4 gene, coding for a tRNA-modifying enzyme, leads to reduced levels of guanosine methylation in tRNA in patients with primordial dwarfism. Guanosine WD repeat domain 4 Homo sapiens