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#618776 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 34; MC1DN34
Cytogenetic locations: 27499296
Gene summaries Genetic tests Medical literature
*618461 - NADH DEHYDROGENASE (UBIQUINONE) COMPLEX I, ASSEMBLY FACTOR 8; NDUFAF8
#616224 - MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22
Cytogenetic locations: 24610330
*609559 - CALMODULIN LYSINE N-METHYLTRANSFERASE; CAMKMT
Cytogenetic locations: 15913950
*609557 - PROLYL ENDOPEPTIDASE-LIKE; PREPL
#606407 - HYPOTONIA-CYSTINURIA SYNDROME
HOMOZYGOUS 2p21 DELETION SYNDROME, INCLUDED
*603770 - PROTEIN PHOSPHATASE, MAGNESIUM/MANGANESE-DEPENDENT, 1B; PPM1B
Cytogenetic locations: Protein
*603196 - COCHLIN; COCH
Cytogenetic locations: 610528
*601097 - PERIPHERAL MYELIN PROTEIN 22; PMP22
Cytogenetic locations: 20493460
*104614 - SOLUTE CARRIER FAMILY 3 (CYSTINE, DIBASIC, AND NEUTRAL AMINO ACID TRANSPORTER), MEMBER 1; SLC3A1
Cytogenetic locations: 17698775
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