Homozygous HOXB1 loss-of-function mutation in a large family with hereditary congenital facial paresis
- 期刊名称American Journal of Medical Genetics Part A
- 作者Vogel, Markus; Velleuer, Eunike; Schmidt-Jiménez, Leon F.; Mayatepek, Ertan; Borkhardt, Arndt; Alawi, Malik; Kutsche, Kerstin; Kortüm, Fanny
- 卷第170卷
- 期第7期
- 印刷ISSN1552-4825
- 文件大小853.39KB
- 发表时间2016-07
- DOI10.1002/ajmg.a.37682
- 页码1813-1819
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