Identification of rare PTCH1 nonsense variant causing...

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Genes & Diseases 2020 / 1

Identification of rare PTCH1 nonsense variant causing orofacial cleft in a Chinese family and an up-to-date genotype-phenotype analysis

Zhong, Wenjie, Zhao, Huaxiang, Huang, Wenbin, Zhang, Mengqi, Zhang, Qian, Zhang, Yue, Chen, Chong, Nueraihemaiti, Zulihumaer, Tuerhong, Dilifeire, Huang, Huizhe, Maimaitili, Gulibaha, Chen, Feng, Lin,
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Journal:
Genes & Diseases
DOI:
10.1016/j.gendis.2019.12.010
Date:
January, 2020
File:
PDF, 1.69 MB
2020
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