protein arginine N-methyltransferase 7 isoform X14 [Homo sapiens]

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The exquisite specificity of human protein arginine methyltransferase 7 (PRMT7) toward Arg-X-Arg sites. [PLoS One. 2023]
The exquisite specificity of human protein arginine methyltransferase 7 (PRMT7) toward Arg-X-Arg sites.
Bondoc TJ, Lowe TL, Clarke SG. PLoS One. 2023; 18(5):e0285812. Epub 2023 May 22.
Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities. [Genet Med. 2023]
Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities.
Cali E, Suri M, Scala M, Ferla MP, Alavi S, Faqeih EA, Bijlsma EK, Wigby KM, Baralle D, Mehrjardi MYV, et al. Genet Med. 2023 Jan; 25(1):135-142. Epub 2022 Nov 18.
Short stature in PRMT7 Mutations: first evidence of response to growth hormone treatment. [Eur J Hum Genet. 2023]
Short stature in PRMT7 Mutations: first evidence of response to growth hormone treatment.
Rodari G, Villa R, Porro M, Gangi S, Iascone M, Elli F, Giacchetti F, Profka E, Collini V, Dall'Antonia A, et al. Eur J Hum Genet. 2023 Feb; 31(2):195-201. Epub 2022 Nov 9.

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protein arginine N-methyltransferase 7 isoform 5 [Homo sapiens]
protein arginine N-methyltransferase 7 isoform 5 [Homo sapiens]
gi|1189131284|ref|NP_001338073.1|

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