Complexome profiling of brain mitochondrial membranes from Clpp-/- mouse
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https://www.omicsdi.org/dataset/pride/PXD025478
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资源简介：
The autosomal recessive Perrault syndrome with juvenile ovarian failure, progressive sensorineural deafness, ataxia and leukoencephalopathy can be caused by loss of function mutations in CLPP. This gene encodes a peptidase that is conserved since bacteria and localizes to mitochondrial matrix in eukaryotes. Here, assembly and stability of mitochondrial complexes from adult Clpp-/- mouse brains were analyzed by Complexome profiling.
创建时间：
2022-02-17
