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  • Biallelic Variants in TMEM17 Cause Meckel‐Gruber Syndrome Within the Ciliopathy Spectrum
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Biallelic Variants in TMEM17 Cause Meckel‐Gruber Syndrome Within the Ciliopathy Spectrum

Fuente: Wiley Open Access
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Bibliographic Details
Main Authors: Luba M. Pardo, Javier Martini, Emir Zonic, Ligia S. Almeida, Maria Iqbal, Mukunth Sadagopan, Alejandra P. Reyes, Nayla Y. León, Mohthash Musambil, Majid Alfadhel, Farhan Javed Dar, Fadwah Tahir, Eman AlSulmi, Nourah Al Qahtani, Hatoon Ahmed Al Taifi, Mohammad Al Hamad, Bader Alhaddad, Sondos Almubayedh, Lama Alabdi, Fowzan S. Alkuraya, Brahim Tabarki, Amal Tawhari, Amal Alhashem, Peter Bauer, Aida Bertoli‐Avella
Format: Artículo Open Access
Published: Wiley 2025
Subjects:
Clinical Genetics
Online Access:
Acceder al recurso
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Internet

https://onlinelibrary.wiley.com/doi/10.1111/cge.14767

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