%0 Letter
%T Diagnostic challenge between a frequent polygenic hypocholesterolemia and an unusual Smith Lemli Opitz syndrome related to bi-allelic DHCR7 mutations.
%A Bonnot Ruget M
%A Moulin P
%A Pagan C
%A Cheillan D
%A Marmontel O
%A Raverot G
%A Benlian P
%A Di Filippo M
%J Clin Chem Lab Med
%V 62
%N 9
%D 2024 Aug 27
%M 38581293
%F 8.49
%R 10.1515/cclm-2024-0162