Heterozygous mutations in the straitjacket region of the latency-associated peptide domain of TGFB2 cause Camurati–Engelmann disease type II-Reference-Cited by-同舟云学术

Heterozygous mutations in the straitjacket region of the latency-associated peptide domain of TGFB2 cause Camurati–Engelmann disease type II

Published:2024-07-16 Issue: Volume: Page:
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Wang Zheng^ORCID,Kometani Mitsuhiro,Zeitlin Leonid,Wilnai Yael,Kinoshita Akira^ORCID,Yoshiura Koh-ichiro^ORCID,Ninomiya Hiroko,Imamura Takeshi,Guo Long^ORCID,Xue Jingyi,Yan Li,Ohashi Hirofumi,Pretemer Yann,Kawai Shunsuke,Shiina Masaaki,Ogata Kazuhiro^ORCID,Cohn Daniel H.,Matsumoto Naomichi^ORCID,Nishimura Gen,Toguchida Junya,Miyake Noriko^ORCID,Ikegawa Shiro

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s10038-024-01274-1.pdf

Reference21 articles.

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5. Ghadami M, Makita Y, Yoshida K, Nishimura G, Fukushima Y, Wakui K, et al. Genetic mapping of the Camurati–Engelmann disease locus to chromosome 19q13.1-q13.3. Am J Hum Genet. 2000;66:143–7.