DOI:
10.1055/s-00000041
Neuropediatrics
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References
Wassiff CA, Maslen C, Kachilele-Linjewile S, Lin D, Linck LM, Conner WE. et al.
Mutations in the human sterol Δ7-reductase gene at 11 q12 - 13 cause Smith-Lemli-Opitz syndrome.
Am J Hum Genet 1998; 63: 55-62
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