mitochondrial inner membrane protease subunit 2 isoform c [Homo sapien - Protein

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Exonic deletions in IMMP2L in schizophrenia with enhanced glycation stress subtype. [PLoS One. 2022]
Exonic deletions in IMMP2L in schizophrenia with enhanced glycation stress subtype.
Yoshikawa A, Kushima I, Miyashita M, Suzuki K, Iino K, Toriumi K, Horiuchi Y, Kawaji H, Ozaki N, Itokawa M, et al. PLoS One. 2022; 17(7):e0270506. Epub 2022 Jul 1.
Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay. [Cytogenet Genome Res. 2021]
Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay.
Vasilyev SA, Skryabin NA, Kashevarova AA, Tolmacheva EN, Savchenko RR, Vasilyeva OY, Lopatkina ME, Zarubin AA, Fishman VS, Belyaeva EO, et al. Cytogenet Genome Res. 2021; 161(3-4):105-119. Epub 2021 Apr 13.
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder. [Cytogenet Genome Res. 2018]
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder.
Baldan F, Gnan C, Franzoni A, Ferino L, Allegri L, Passon N, Damante G. Cytogenet Genome Res. 2018; 154(4):196-200. Epub 2018 May 23.

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Protein