Ma_1991_N.Engl.J.Med_324_1761

Reference

Title : A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians - Ma_1991_N.Engl.J.Med_324_1761
Author(s) : Ma Y , Henderson HE , Murthy V , Roederer G , Monsalve MV , Clarke LA , Normand T , Julien P , Gagne C , Lambert M , et al.
Ref : N Engl J Med , 324 :1761 , 1991
Abstract : Ma_1991_N.Engl.J.Med_324_1761
ESTHER : Ma_1991_N.Engl.J.Med_324_1761
PubMedSearch : Ma_1991_N.Engl.J.Med_324_1761
PubMedID: 2038366
Gene_locus related to this paper: human-LPL

Related information

Gene_locus related to this paper: human-LPL

Citations formats

Ma Y, Henderson HE, Murthy V, Roederer G, Monsalve MV, Clarke LA, Normand T, Julien P, Gagne C, Lambert M, et al. (1991)
A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians
N Engl J Med 324 :1761

Ma Y, Henderson HE, Murthy V, Roederer G, Monsalve MV, Clarke LA, Normand T, Julien P, Gagne C, Lambert M, et al. (1991)
N Engl J Med 324 :1761