Gene Locus : human-PPT1
Mode of mutation : Natural mutant
Disease : Infantile neuronal ceroid lipofuscinosis
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 :
Aberrant splicing of intron 7 c.727-2A>T CS982326
Title : Molecular genetics of palmitoyl-protein thioesterase deficiency in the U.S - Das_1998_J.Clin.Invest_102_361 |
Author(s) : Das AK , Becerra CH , Yi W , Lu JY , Siakotos AN , Wisniewski KE , Hofmann SL |
Ref : Journal of Clinical Investigation , 102 :361 , 1998 |
Abstract : |
PubMedSearch : Das_1998_J.Clin.Invest_102_361 |
PubMedID: 9664077 |
Gene_locus related to this paper: human-PPT1 |