Single-Cell Transcriptome Analysis Defines Expression of Kabuki Syndrome-Associated KMT2D Targets and Interacting Partners

Objectives. Kabuki syndrome (KS) is a rare genetic disorder characterized by developmental delay, retarded growth, and cardiac, gastrointestinal, neurocognitive, renal, craniofacial, dental, and skeletal defects. KS is caused by mutations in the genes encoding histone H3 lysine 4 methyltransferase (...

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Detalles Bibliográficos
Autores principales: Enkhmandakh, Badam, Robson, Paul, Joshi, Pujan, Vijaykumar, Anushree, Shin, Dong-Guk, Mina, Mina, Bayarsaihan, Dashzeveg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9391158/
https://www.ncbi.nlm.nih.gov/pubmed/35992033
http://dx.doi.org/10.1155/2022/4969441

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9391158/
https://www.ncbi.nlm.nih.gov/pubmed/35992033
http://dx.doi.org/10.1155/2022/4969441

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