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|Query Trace: Smith-Lemli-Opitz Syndrome and ABCA1[original query]|
| Maternal ABCA1 genotype is associated with severity of Smith-Lemli-Opitz syndrome and with viability of patients homozygous for null mutations.
European journal of human genetics : EJHG 2012 Aug .
Lanthaler B, Steichen-Gersdorf E, Kollerits B, Zschocke J, Witsch-Baumgartner M
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