doi.org/10.1111/cge.14084

DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition

Naama Orenstein

,

..., Lina Basel-Salmon

Clinical Genetics3.50

Volume: 101, Issue: 2, Pages: 265 - 266

Published: Nov 16, 2021

Abstract

A family with DYRK1B LOF variant offering to expand the phenotype beyond the metabolic...

Paper Fields

Paper Details

Title

DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition

DOI

doi.org/10.1111/cge.14084

Published Date

Nov 16, 2021

Journal

Clinical Genetics

Volume

101

Issue

2

Pages

265 - 266

Citation AnalysisPro

You’ll need to upgrade your plan to Pro

Looking to understand the true influence of a researcher’s work across journals & affiliations?

Scinapse’s Top 10 Citation Journals & Affiliations graph reveals the quality and authenticity of citations received by a paper.
Discover whether citations have been inflated due to self-citations, or if citations include institutional bias.

Notes

History