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Updated: Sep 9, 2025

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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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Otro caso que apoya la PDCD6IP como el gen responsable de un trastorno del desarrollo neurológico con microcefalia
Alfonso Manuel D'Alessio1,2, Annalaura Torella1,3, Manuela Morleo1,4
1Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.
Clinical genetics
|September 2, 2025
Resumen
Este estudio detalla los hallazgos clínicos y moleculares en pacientes con variantes bialélicas del gen PDCD6IP. Comprender estas variaciones genéticas es crucial para el diagnóstico y el manejo de enfermedades relacionadas.
Área de la Ciencia:
- La genética
- Biología molecular
- Medicina Clínica
Sus antecedentes:
- El gen PDCD6IP juega un papel en los procesos celulares.
- Las variantes bialélicas en PDCD6IP pueden conducir a diversas manifestaciones clínicas.
- Comprender la correlación genotipo-fenotipo es esencial para el asesoramiento genético.
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