Kamal_2022_Ther.Adv.Chronic.Dis_13_20406223221078757

Reference

Title : Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family study - Kamal_2022_Ther.Adv.Chronic.Dis_13_20406223221078757
Author(s) : Kamal NM , Saadah OI , Alheraiti SS , Attar R , Alsufyani AD , El-Shabrawi MHF , Sherief LM
Ref : Ther Adv Chronic Dis , 13 :20406223221078757 , 2022
Abstract : Kamal_2022_Ther.Adv.Chronic.Dis_13_20406223221078757
ESTHER : Kamal_2022_Ther.Adv.Chronic.Dis_13_20406223221078757
PubMedSearch : Kamal_2022_Ther.Adv.Chronic.Dis_13_20406223221078757
PubMedID: 35284057
Gene_locus related to this paper: human-PNLIP

Related information

Gene_locus related to this paper: human-PNLIP

Citations formats

Kamal NM, Saadah OI, Alheraiti SS, Attar R, Alsufyani AD, El-Shabrawi MHF, Sherief LM (2022)
Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family study
Ther Adv Chronic Dis 13 :20406223221078757

Kamal NM, Saadah OI, Alheraiti SS, Attar R, Alsufyani AD, El-Shabrawi MHF, Sherief LM (2022)
Ther Adv Chronic Dis 13 :20406223221078757