PDGFRB mutation causes autosomal-dominant Penttinen syndrome

10.1111/cge.12680

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Bibliographic Details
Main Author: Aminkeng, F
Other Authors: MEDICINE
Format: Article
Language:English
Published: WILEY-BLACKWELL 2022
Subjects:
Online Access:https://scholarbank.nus.edu.sg/handle/10635/235098
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Institution: National University of Singapore
Language: English

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