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:https://doi.org/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

Tel Aviv University

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

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

All Science Journal Classification (ASJC) codes

Genetics(clinical)
Genetics

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https://doi.org/10.1111/cge.14084

Cite this

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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",

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doi = "https://doi.org/10.1111/cge.14084",

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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

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U2 - https://doi.org/10.1111/cge.14084

DO - https://doi.org/10.1111/cge.14084

M3 - رسالة

C2 - 34786696

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

All Science Journal Classification (ASJC) codes

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