O'Donnel‑Luria‑Rodan Syndrome: New gene variant identified in Romania (A case report)-Reference-Cited by-同舟云学术

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O'Donnel‑Luria‑Rodan Syndrome: New gene variant identified in Romania (A case report)

Published:2022-04-04 Issue:5 Volume:23 Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Cătană Andreea¹,Kutasi Enikő¹,Cuzmici‑Barabaș Zina²,Militaru Diana²,Iordănescu Irina³,Militaru Mariela²

Affiliation:

1. Department of Oncogenetics, Institute of Oncology I. Chiricuță, Cluj‑Napoca, Transylvania 4000015, Romania

2. Department of Molecular Sciences, University of Medicine and Pharmacy, Cluj‑Napoca, Transylvania 4000012, Romania

3. Department of Medical Genetics, Genetic Center Laboratory, Regina Maria, Bucharest 011376, Romania

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Reference14 articles.

1. MLL5 (KMT2E): Structure, function, and clinical relevance;Zhang;Cell Mol Life Sci,2017

2. Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy;O'Donnell-Luria;Am J Hum Genet,2019

3. Regulation of histone H3K4 methylation in brain development and disease;Shen;Philos Trans R Soc Lond B Biol Sci,2014

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