DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition

Naama Orenstein; Yoel Gofin; Noam Shomron; Noa Ruhrman-Shahar; Nurit Magal; Ofir Hagari; Noy Azulay; Lily Bazak; Yael Goldberg; Lina Basel-Salmon

doi:10.1111/cge.14084

DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition

Naama Orenstein^*, Yoel Gofin, Noam Shomron, Noa Ruhrman-Shahar, Nurit Magal, Ofir Hagari, Noy Azulay, Lily Bazak, Yael Goldberg, Lina Basel-Salmon

^*Corresponding author for this work

Research output: Contribution to journal › Letter › peer-review

4 Scopus citations

Original language	English
Pages (from-to)	265-266
Number of pages	2
Journal	Clinical Genetics
Volume	101
Issue number	2
DOIs	https://doi.org/10.1111/cge.14084
State	Published - Feb 2022

Access to Document

10.1111/cge.14084

Cite this

@article{93f2a50a8cdc4a698874d1e05fbfa8ca,

title = "DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition",

author = "Naama Orenstein and Yoel Gofin and Noam Shomron and Noa Ruhrman-Shahar and Nurit Magal and Ofir Hagari and Noy Azulay and Lily Bazak and Yael Goldberg and Lina Basel-Salmon",

year = "2022",

month = feb,

doi = "10.1111/cge.14084",

language = "אנגלית",

volume = "101",

pages = "265--266",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "2",

}

TY - JOUR

T1 - DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition

AU - Orenstein, Naama

AU - Gofin, Yoel

AU - Shomron, Noam

AU - Ruhrman-Shahar, Noa

AU - Magal, Nurit

AU - Hagari, Ofir

AU - Azulay, Noy

AU - Bazak, Lily

AU - Goldberg, Yael

AU - Basel-Salmon, Lina

PY - 2022/2

Y1 - 2022/2

UR - http://www.scopus.com/inward/record.url?scp=85119043366&partnerID=8YFLogxK

U2 - 10.1111/cge.14084

DO - 10.1111/cge.14084

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.letter???

C2 - 34786696

AN - SCOPUS:85119043366

SN - 0009-9163

VL - 101

SP - 265

EP - 266

JO - Clinical Genetics

JF - Clinical Genetics

IS - 2

ER -

DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition

Access to Document

Other files and links

Cite this