Genetic etiology and clinical challenges of phenylketonuria

NA Elhawary, IA AlJahdali, IS Abumansour… - Human genomics, 2022 - Springer
This review discusses the epidemiology, pathophysiology, genetic etiology, and
management of phenylketonuria (PKU). PKU, an autosomal recessive disease, is an inborn …

PWAS Hub: Exploring Gene-Based Associations of Common Complex Diseases

G Kelman, R Zucker, N Brandes, M Linial - medRxiv, 2024 - medrxiv.org
PWAS (Proteome-Wide Association Study) is an innovative genetic association approach
that complements widely-used methods like GWAS (Genome-Wide Association Study). The …

[PDF][PDF] ASOCIACIÓN DE LOS POLIMORFISMOS LMP2 RS17587 Y LMP7 RS2071543 EN TEJIDOS DE PACIENTES CON LINFOMAS HODGKIN Y NO HODGKIN …

MKCL LASTEROS - riudg.udg.mx
Los virus son los microorganismos infecciosos más pequeños del mundo, son considerados
parásitos genéticos intracelulares obligados, y entre sus distinciones más importantes …

[PDF][PDF] Assessment of knowledge and perception towards vitiligo in Northern Saudi Arabia

FF Alreshidi, ES Almughais, D Alayed, RM Alarfaj… - 2022 - discoveryjournals.org
Background: There is a prevalence of vitiligo in Saudi Arabia, with low reports regarding the
burden of the disease. Thus, the current study aimed to assess the knowledge and …