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#616224 - MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22
Cytogenetic locations: 600572
Gene summaries Genetic tests Medical literature
*609559 - CALMODULIN LYSINE N-METHYLTRANSFERASE; CAMKMT
Cytogenetic locations: 15913950
*609557 - PROLYL ENDOPEPTIDASE-LIKE; PREPL
#606407 - HYPOTONIA-CYSTINURIA SYNDROME
HOMOZYGOUS 2p21 DELETION SYNDROME, INCLUDED
Cytogenetic locations: 24610330
*603770 - PROTEIN PHOSPHATASE, MAGNESIUM/MANGANESE-DEPENDENT, 1B; PPM1B
*603196 - COCHLIN; COCH
Cytogenetic locations: 18312449
*601097 - PERIPHERAL MYELIN PROTEIN 22; PMP22
Cytogenetic locations: 605398
*104614 - SOLUTE CARRIER FAMILY 3 (CYSTINE, DIBASIC, AND NEUTRAL AMINO ACID TRANSPORTER), MEMBER 1; SLC3A1
Cytogenetic locations: 2p22.1
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