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Paper Report for: 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 NM, Saadah OI, Alheraiti SS, Attar R, Alsufyani AD, El-Shabrawi MHF, Sherief LM
Ref: Ther Adv Chronic Dis, 13:20406223221078757, 2022 : PubMed

        



Related information

Gene_Locus| human-PNLIP
Mutation | W419X_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



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