{Reference Type}: Letter
{Title}: Diagnostic challenge between a frequent polygenic hypocholesterolemia and an unusual Smith Lemli Opitz syndrome related to bi-allelic DHCR7 mutations.
{Author}: Bonnot Ruget M;Moulin P;Pagan C;Cheillan D;Marmontel O;Raverot G;Benlian P;Di Filippo M;
{Journal}: Clin Chem Lab Med
{Volume}: 62
{Issue}: 9
{Year}: 2024 Aug 27
{Factor}: 8.49
{DOI}: 10.1515/cclm-2024-0162