A novel two bases deletion in the albumin gene causes analbuminaemia in a young Turkish man-Reference-Cited by-同舟云学术

A novel two bases deletion in the albumin gene causes analbuminaemia in a young Turkish man

Published:2012-05 Issue:9-10 Volume:413 Page:950-951
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Caridi Gianluca,Dagnino Monica,Di Duca Marco,Akyuz Filiz,Boztas Gungor,Besisik Fatih,Demir Kadir,Ormeci Asli,Gokturk Suut,Cefle Kivanc,Ozturk Şukru,Palanduz Sukru,Campagnoli Monica,Galliano Monica,Minchiotti Lorenzo

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference9 articles.

1. All about albumin: biochemistry, genetics and medical applications;Peters,1996

2. A novel splicing mutation causes analbuminemia in a Portuguese boy;Caridi;Mol Genet Metab,2012

3. Mutations and polymorphisms of the gene of the major human blood protein, serum albumin;Minchiotti;Hum Mutat,2008

4. A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman;Dagnino;Clin Chim Acta,2010

5. Molecular structure of the human albumin gene is revealed by nucleotide sequence within q11–22 of chromosome 4;Minghetti;J Biol Chem,1986

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia;Frontiers in Genetics;2019-04-17

2. Analbuminaemia: clinical features and associated hypercholesterolaemia;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;2016-07-19

3. A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family;Biochemia Medica;2016

4. Molecular Genetics of Analbuminaemia;eLS;2014-01-15

5. Congenital analbuminaemia: Molecular defects and biochemical and clinical aspects;Biochimica et Biophysica Acta (BBA) - General Subjects;2013-12