RNA recognition motif of LEMD3 as a key player in the pathogenesis of Buschke–Ollendorff syndrome
Author:
Publisher
Elsevier BV
Subject
Dermatology,Molecular Biology,Biochemistry
Reference10 articles.
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3. Loss-of-function mutations in LEMD3 result in osteopoikilosis, Bushcke–Ollendorff syndrome and melorheostosis;Hellemans;Nat. Genet.,2004
4. XMAN1, an inner nuclear membrane protein, antagonizes BMP signaling by interacting with Smad1 in Xenopus embryos;Osada;Development,2003
5. Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively—coincidence within one family;Baasanjav;BMC Med. Genet.,2010
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1. Buschke‐Ollendorff syndrome with LEMD3 germline stopgain mutation p. R678 * presenting as multiple subcutaneous nodules with mucin deposition;Journal of Cutaneous Pathology;2020-07-04
2. Buschke–Ollendorff Syndrome, Marfan Syndrome and Osteogenesis Imperfecta;Harper's Textbook of Pediatric Dermatology;2019-11-20
3. Cutaneous Elastic Tissue Anomalies;The American Journal of Dermatopathology;2019-02
4. Helen Ollendorff Curth: A dermatologist’s lasting legacy;International Journal of Women's Dermatology;2017-03
5. Helen Ollendorff-Curth: A dermatologist’s lasting legacy;International Journal of Women's Dermatology;2016-09
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