লোডিং...
Identification and In Vitro Functional Verification of Two Novel Mutations of GHR Gene in the Chinese Children with Laron Syndrome
PURPOSE: Laron syndrome (LS) is a severe growth disorder caused by GHR gene mutation or post-receptor pathways defect. The clinical features of these patients collected in our present study were summarized, GHR gene variants were investigated and further in vitro functional verification was carried...
সংরক্ষণ করুন:
| প্রকাশিত: | Front Endocrinol (Lausanne) |
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| প্রধান লেখক: | , , , , , , , , , , |
| বিন্যাস: | Artigo |
| ভাষা: | Inglês |
| প্রকাশিত: |
Frontiers Media S.A.
2021
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| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8072467/ https://ncbi.nlm.nih.gov/pubmed/33912130 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2021.605736 |
| ট্যাগগুলো: |
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