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Narooie–Nejad M et al. – Observation of the absence of linkage to GLC3B and GLC3C in at least nine families without CYP1B1 mutations suggests that at least one PCG–causing locus other than GLC3A, GLC3B, and GLC3C may exist. The disease–causing gene or genes in the novel locus or loci may account for PCG in a notable fraction of Iranian patients.

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