DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
van Rahden VA, Fernandez-Vizarra E, Alawi M. , et al.
Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome.
Am J Hum Genet 2015;
96 (04) 640-650
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