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<< < Results 31 - 36 of 36
EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Microcephaly
TRMT10A mutation in a child with diabetes, short stature, microcephaly and hypoplastic kidneys.
causal interaction
unassigned
3
0
Microcephaly
tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans.
causal interaction
ongoing research
therapeutic application
unassigned
4
1
1
0
Microcephaly
tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy.
causal interaction
ongoing research
therapeutic application
unassigned
4
1
3
0
Microcephaly
Pancreatic ?-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes.
causal interaction
ongoing research
unassigned
4
2
0
Microcephaly
tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly.
causal interaction
ongoing research
unassigned
4
1
0
Microcephaly
Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases.
causal interaction
unassigned
4
0
<< < Results 31 - 36 of 36