PREPL: a putative novel oligopeptidase propelled into the limelight
Author:
Publisher
Walter de Gruyter GmbH
Subject
Clinical Biochemistry,Molecular Biology,Biochemistry
Link
https://www.degruyter.com/document/doi/10.1515/BC.2006.111/pdf
Reference26 articles.
1. Molecular analysis of the cystinuria disease gene: identification of four new mutations, one large deletion, and one polymorphism
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3. New insights into cystinuria: 40 new mutations, genotype-phenotype correlation, and digenic inheritance causing partial phenotype
4. Prolyl Oligopeptidase
5. Catalysis of serine oligopeptidases is controlled by a gating filter mechanism
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2. Prolyl endopeptidase-like is a (thio)esterase involved in mitochondrial respiratory chain function;iScience;2021-12
3. Prolyl Endopeptidase-like (PREPL) Deficiency Associated with Growth Hormone Deficiency: Case Report;Journal of Clinical Research in Pediatric Endocrinology;2021-10-25
4. First maternal uniparental disomy for chromosome 2 with PREPL novel frameshift mutation of congenital myasthenic syndrome 22 in an infant;Molecular Genetics & Genomic Medicine;2020-01-27
5. The Neuromuscular Junction and Wide Heterogeneity of Congenital Myasthenic Syndromes;International Journal of Molecular Sciences;2018-06-05
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