FIGURE

Fig. 1

ID

ZDB-FIG-251223-20

Publication

Kröll-Hermi et al., 2025 - Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability

Other Figures

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Fig. 1

Individuals and variants identified in PRMT9 (A) Schematic of the PRMT9 locus, mRNA, and protein with the different protein domains. Variation positions are given according to the RefSeq identifiers GenBank: NM_138364.3 and NP_612373.2. (B) Face (upper) and profile (lower) photographs for individuals with bi-allelic pathogenic variant in PRMT9 for families C, F, G, J, K, W, and X.

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Phenotype Detail

Acknowledgments

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