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 : c.684delT p.(Phe22LeufsTer13) LIPA exon 4 deletion (frameshift)compound heterozygous
| Title : Enzyme replacement therapy and hematopoietic stem cell transplant: a new paradigm of treatment in Wolman disease - Potter_2021_Orphanet.J.Rare.Dis_16_235 |
| Author(s) : Potter JE , Petts G , Ghosh A , White FJ , Kinsella JL , Hughes S , Roberts J , Hodgkinson A , Brammeier K , Church H , Merrigan C , Hughes J , Evans P , Campbell H , Bonney D , Newman WG , Bigger BW , Broomfield A , Jones SA , Wynn RF |
| Ref : Orphanet J Rare Dis , 16 :235 , 2021 |
| Abstract : Potter_2021_Orphanet.J.Rare.Dis_16_235 |
| ESTHER : Potter_2021_Orphanet.J.Rare.Dis_16_235 |
| PubMedSearch : Potter_2021_Orphanet.J.Rare.Dis_16_235 |
| PubMedID: 34020687 |
| Gene_locus related to this paper: human-LIPA |