Turnitin 降AI改写 早检测系统 早降重系统 Turnitin-UK版 万方检测-期刊版 维普编辑部版 Grammarly检测 Paperpass检测 checkpass检测 PaperYY检测
[Free GPT-4]
[DeepSeek]
[PDF] mdpi.com

A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families

M Aldosary, M Alsagob, H AlQudairy… - Cells, 2022 - mdpi.com
The genetic architecture of mitochondrial disease continues to expand and currently
exceeds more than 350 disease-causing genes. Bi-allelic variants in RTN4IP1, also known …
Сохранить Цитировать Цитируется: 2 Похожие статьи Все версии статьи (14) Сохраненная копия

YIF1B-related Kaya-Barakat-Masson Syndrome: Report of a new patient and literature review

A Sanri, MB Mutlu, O Sezer - European Journal of Medical Genetics, 2023 - Elsevier
Abstract Kaya-Barakat-Masson syndrome (KABAMAS) is a recently identified severe
neurodevelopmental disorder characterized by severe global developmental delay …
Сохранить Цитировать Цитируется: 1 Похожие статьи Все версии статьи (3)