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#619303 - PONTOCEREBELLAR HYPOPLASIA, TYPE 1E; PCH1E
Cytogenetic locations: MTX3
Gene summaries Genetic tests Medical literature
#616505 - NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB, WITH OPTIC ATROPHY; HMSN6B
*610826 - SOLUTE CARRIER FAMILY 25, MEMBER 46; SLC25A46
Cytogenetic locations: 27543974
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