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323624
323624
http://dx.doi.org/10.1086/323624
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.
P356
Q24533422-AC5ED5CE-BD5E-41F1-9E43-E29089F18301
P356
323624
http://dx.doi.org/10.1086/323624