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SREP13050
SREP13050
http://dx.doi.org/10.1038/SREP13050
Point mutations in KAL1 and the mitochondrial gene MT-tRNA(cys) synergize to produce Kallmann syndrome phenotype.
P356
Q36273551-05A37456-9C60-4A2A-BCDE-5C9333E1CE39
P356
SREP13050
http://dx.doi.org/10.1038/SREP13050