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Product

NSD1 mutations deregulate transcription and DNA methylation of bivalent developmental genes in Sotos syndrome

Center:

AR-Partners for Inclusive Communities, UCEDD/LEND

Fiscal Year:

2022

Contact Information:

Renee Holmes
[email protected]
479-871-2836

Product Description:

Sotos syndrome (SS), the most common overgrowth with intellectual disability (OGID) disorder, is caused by inactivating germline mutations of NSD1, which encodes a histone H3 lysine 36 methyltransferase.

Keyword(s):

Product/Publication Type(s):

Peer-reviewed publications in scholarly journals Published/In Press

Target Audience:

Policymakers

Alternative Format:

Electronic (disc, CD, 508 compliant web posting)

To Obtain Copies (URL or Email):

https://pubmed.ncbi.nlm.nih.gov/35094088/

COVID-19 Related Data:

N/A

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