Gene Locus : human-LIPA
Mode of mutation : Natural mutant
Disease : Wolman disease WD, Cholesterol Ester Storage Disease, CESD
Summary :
AAA Change :
Allelic Variant :
Risk Factor :
Inhibitor :
Structure :
Disease by interaction :
Interact Gene Locus :
Xenobiotic sensitivity :
Modification :
Torpedo_number : No torpedo number
Kinetic Parameter : No kinetic parameter
News : No news
Comment : p.Ile41LeufsTer4 p.I41LfsX4 c.119_126del. A compound heterozygous for an 8-bp deletion in exon 3 159-166del (TTATCTCT) (and a 2-bp deletion in exon 4) These frameshift mutations lead to at amino acid positions 45(24) and 116. c.119_126del, p.Ile20LeufsTer4 p.I20LfsX4 Ex3_8del_24X
| Title : Molecular defects underlying Wolman disease appear to be more heterogeneous than those resulting in cholesteryl ester storage disease - Lohse_1999_J.Lipid.Res_40_221 |
| Author(s) : Lohse P , Maas S , Sewell AC , van Diggelen OP , Seidel D |
| Ref : J Lipid Res , 40 :221 , 1999 |
| Abstract : Lohse_1999_J.Lipid.Res_40_221 |
| ESTHER : Lohse_1999_J.Lipid.Res_40_221 |
| PubMedSearch : Lohse_1999_J.Lipid.Res_40_221 |
| PubMedID: 9925650 |
| Gene_locus related to this paper: human-LIPA |