| Title : Familial lipoprotein lipase deficiency in infancy: clinical, biochemical, and molecular study - Feoli-Fonseca_1998_J.Pediatr_133_417 |
| Author(s) : Feoli-Fonseca JC , Levy E , Godard M , Lambert M |
| Ref : J Pediatr , 133 :417 , 1998 |
| Abstract : |
| PubMedSearch : Feoli-Fonseca_1998_J.Pediatr_133_417 |
| PubMedID: 9738727 |
| Title : Expression of the transcripts initiated in the 62nd intron of the dystrophin gene - Lambert_1993_Neuromuscul.Disord_3_519 |
| Author(s) : Lambert M , Chafey P , Hugnot JP , Koulakoff A , Berwald-Netter Y , Billard C , Morris GE , Kahn A , Kaplan JC , Gilgenkrantz H |
| Ref : Neuromuscular Disorders , 3 :519 , 1993 |
| Abstract : |
| PubMedSearch : Lambert_1993_Neuromuscul.Disord_3_519 |
| PubMedID: 8186704 |
| 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 : |
| PubMedSearch : Ma_1991_N.Engl.J.Med_324_1761 |
| PubMedID: 2038366 |
| Gene_locus related to this paper: human-LPL |