دورية أكاديمية
A novel heterozygous mutation of CHD7 gene in a Chinese patient with Kallmann syndrome: a case report
العنوان: | A novel heterozygous mutation of CHD7 gene in a Chinese patient with Kallmann syndrome: a case report |
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المؤلفون: | Xu, Weiwei, Zhou, Weibin, Lin, Haiyang, Ye, Dan, Chen, Guoping, Dong, Fengqin, Shen, JianguoAff1 |
المصدر: | BMC Endocrine Disorders. 21(1) |
قاعدة البيانات: | Springer Nature Journals |
تدمد: | 14726823 |
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DOI: | 10.1186/s12902-021-00836-0 |