The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease)

标题
The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease)
作者
关键词
-
出版物
JOURNAL OF HUMAN GENETICS
Volume 53, Issue 10, Pages 947-949
出版商
Springer Nature
发表日期
2008-08-12
DOI
10.1007/s10038-008-0328-5

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