EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.4.24.64 | Cerebellar Ataxia |
25808372 |
PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia. |
causal interaction
unassigned |
3
0 |
| 3.4.24.64 | Cerebellar Ataxia |
26657514 |
Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA. |
causal interaction
unassigned |
4
0 |
| 3.4.24.64 | Cerebellar Ataxia |
26657516 |
Reply: Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA. |
causal interaction
unassigned |
4
0 |
| 3.4.24.64 | Filariasis |
16788047 |
Identification and reverse genetic analysis of mitochondrial processing peptidase and the core protein of the cytochrome bc1 complex of Caenorhabditis elegans, a model parasitic nematode. |
ongoing research
unassigned |
3
0 |
| 3.4.24.64 | Spinocerebellar Ataxias |
33272776 |
A severe form of autosomal recessive spinocerebellar ataxia associated with novel PMPCA variants. |
causal interaction
unassigned |
3
0 |
