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A Model for Spinal Muscular Atrophy Disease Registry for Iran

Objective(s): Spinal muscular atrophy is a rare genetic disease of neuromuscular and it is considered the main cause of death of newborns, which affects spinal motor neurons. The variety of degrees of this disease and the lack of a complete and integrated information recording system hinder the qual...

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Bibliografiske detaljer
Principais autores: Hadiseh Azadi Cheshmekabodi, Farahnaz Sadoughi, Somayeh Nasiri
Format: Artigo
Sprog:Persa
Udgivet: Iranian Institute for Health Sciences Research 2025-08-01
Serier:Payesh
Fag:
Online adgang:http://payeshjournal.ir/article-1-2576-en.pdf
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