DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Wimplinger I, Morleo M, Rosenberger G. , et al.
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.
Am J Hum Genet 2006;
79 (05) 878-889
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