D352del_human-LIPA

General

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.D352del D352del c.1055_1057del found in a compound heterozygote with with H129R

References (2)

Title : First LIPA Mutational Analysis in Egyptian Patients Reveals One Novel Variant: Wolman Disease - Elaraby_2023_J.Mol.Neurosci__
Author(s) : Elaraby NM , Galal ER , Abdel-Hamid M , Elbendary HM , Elbadry M , Mekkawy MK , Ashaat NA , Mounir SM , Ashaat EA
Ref : Journal of Molecular Neuroscience , : , 2023
Abstract : Elaraby_2023_J.Mol.Neurosci__
ESTHER : Elaraby_2023_J.Mol.Neurosci__
PubMedSearch : Elaraby_2023_J.Mol.Neurosci__
PubMedID: 37470904
Gene_locus related to this paper: human-LIPA

Title : Lysosomal Acid Lipase Deficiency in 23 Spanish Patients: High Frequency of the Novel c.966+2T>G Mutation in Wolman Disease - Ruiz-Andres_2017_JIMD.Rep_37_7
Author(s) : Ruiz-Andres C , Selles E , Arias A , Gort L
Ref : JIMD Rep , 37 :7 , 2017
Abstract : Ruiz-Andres_2017_JIMD.Rep_37_7
ESTHER : Ruiz-Andres_2017_JIMD.Rep_37_7
PubMedSearch : Ruiz-Andres_2017_JIMD.Rep_37_7
PubMedID: 28220406
Gene_locus related to this paper: human-LIPA