NDUFB11

Publications

Indrieri A et al.  Linear Skin Defects with Multiple Congenital Anomalies (LSDMCA): An Unconventional Mitochondrial Disorder. Genes. 2021;12(2):263. PMID: 33670341.

van Rahden V 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(4):640-50. PMID: 25772934.