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White matter disorders and cerebral calcification - narrow panel v2.5 | COX15 | Arina Puzriakova Phenotypes for gene: COX15 were changed from Mitochondrial complex IV disorders; Mitochondrial Leukoencephalopathy to Mitochondrial complex IV deficiency, nuclear type 6, OMIM:615119; Mitochondrial Leukoencephalopathy | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
White matter disorders and cerebral calcification - narrow panel v0.11 | COX15 |
Ellen McDonagh gene: COX15 was added gene: COX15 was added to White matter disorders and cerebral calcification - narrow panel. Sources: Expert Review Green Mode of inheritance for gene: COX15 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: COX15 were set to 25655951 Phenotypes for gene: COX15 were set to Mitochondrial complex IV disorders; Mitochondrial Leukoencephalopathy |