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Results 1 - 3 of 3 for Van den Bosch syndrome
  1. SLC19A3 gene 
    ... I, Coppieters W, Karim L, de Coo R, van den Bosch B, Smeets H. Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome. Brain. 2013 Mar;136(Pt 3):882-90. ...
    https://medlineplus.gov/genetics/gene/slc19a3 - Genetics
  2. COQ8B gene 
    ... or Free article on PubMed Central Gerards M, van den Bosch B, Calis C, Schoonderwoerd K, van Engelen K, Tijssen M, de Coo R, van ...
    https://medlineplus.gov/genetics/gene/coq8b - Genetics
  3. Medium-chain acyl-CoA dehydrogenase deficiency 
    ... Derks TG, Reijngoud DJ, Waterham HR, Gerver WJ, van den Berg MP, Sauer PJ, Smit GP. The natural ...
    https://medlineplus.gov/...m-chain-acyl-coa-dehydrogenase-deficiency - Genetics