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*620765 - MITOCHONDRIAL FISSION REGULATOR 1-LIKE PROTEIN; MTFR1L
Gene summaries Genetic tests Medical literature
*620737 - COENZYME Q10B; COQ10B
*620736 - COENZYME Q10A; COQ10A
#620569 - LEBER-LIKE HEREDITARY OPTIC NEUROPATHY, AUTOSOMAL RECESSIVE 2; LHONAR2
Cytogenetic locations: 606841
#620137 - MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 11; MC3DN11
Cytogenetic locations: P}#<##
#620135 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 39; MC1DN39
Cytogenetic locations: #&#U##
#619828 - SPERMATOGENIC FAILURE 70; SPGF70
Cytogenetic locations: p#####
#619701 - YOON-BELLEN NEURODEVELOPMENTAL SYNDROME; YOBELN
Cytogenetic locations: -
#619425 - MITOCHONDRIAL DNA DEPLETION SYNDROME 16B (NEUROOPHTHALMIC TYPE); MTDPS16B
Cytogenetic locations: #.#J##
*619414 - MITOCHONDRIAL FISSION REGULATOR 1; MTFR1
Cytogenetic locations: Retinitis
#619279 - PARKINSONISM WITH POLYNEUROPATHY; PKNPY
#619272 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 37; MC1DN37
Cytogenetic locations: ###]##
#619259 - NEURODEGENERATION WITH ATAXIA AND LATE-ONSET OPTIC ATROPHY; NDAXOA
Cytogenetic locations: 4q35.1
#619224 - MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 4; MC2DN4
Cytogenetic locations: 0#####
#619170 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 36; MC1DN36
Cytogenetic locations: #Pe###
#619167 - MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 3; MC2DN3
Cytogenetic locations: `#####
#619065 - MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 21; MC4DN21
Cytogenetic locations: RAP
#619064 - MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 20; MC4DN20
Cytogenetic locations: 15q22.31
#619062 - MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 18; MC4DN18
Cytogenetic locations: 613374
#619060 - MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 16; MC4DN16
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