ODLURO syndrome: personal experience and review of the literature-Reference-Cited by-同舟云学术

ODLURO syndrome: personal experience and review of the literature

Published:2020-07-20 Issue:2 Volume:126 Page:316-322
ISSN:0033-8362
Container-title:La radiologia medica
language:en
Short-container-title:Radiol med

Author:

Conforti Renata,Iovine Silvia,Santangelo Gabriella,Capasso Raffaella,Cirillo Mario,Fratta Mario,Caranci Ferdinando^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Radiology, Nuclear Medicine and imaging,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s11547-020-01255-2.pdf

Reference20 articles.

1. O’Donnell-Luria A, Pais L, Faundes V, Wood J, Sveden A, Luria V et al (2019) Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy. Am J Hum Genet 104(6):1210–1222. https://doi.org/10.1016/j.ajhg.2019.03.021

2. Shen E, Shulha H, Weng Z, Akbarian S (2014) Regulation of histone H3K4 methylation in brain development and disease. Philos Trans R Soc Lond B Biol Sci 369(1652):20130514. https://doi.org/10.1098/rstb.2013.0514

3. Larizza L, Finelli P (2019) Developmental disorders with intellectual disability driven by chromatin dysregulation: clinical overlaps and molecular mechanisms. Clin Genet 95(2):231–240. https://doi.org/10.1111/cge.13365

4. Zhang X, Novera W, Zhang Y, Deng LW (2017) MLL5 (KMT2E): structure, function, and clinical relevance. Cell Mol Life Sci 74(13):2333–2344

5. Guz W, Pazdan D, Stachyra S, Swieton F, Poreba P, Bednarz M et al (2019) Analysis of corpus callosum size depending on age and sex. Folia Morphol 78(1):24–32

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