Novel compound heterozygous pathogenic variants in ASCC1 in a Chinese patient with spinal muscular atrophy with congenital bone fractures 2 : Evidence supporting a "Definitive" gene‐disease relationship

BACKGROUND: A very limited spectrum of ASCC1 pathogenic variants had been reported in six (mostly consanguineous) families with spinal muscular atrophy with congenital bone fractures 2 [OMIM #616867] since 2016. METHODS: A proband from a non‐consanguineous Chinese family presented with neonatal seve...

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Detalles Bibliográficos
Autores principales: Lu, Weiliang, Liang, Mingxing, Su, Jiasun, Wang, Jin, Li, Lingxiao, Zhang, Shujie, Qin, Zailong, Huang, Limei, Lu, Yingchi, Yi, Shang, Yi, Sheng, Xie, BoBo, Zheng, Haiyang, Luo, Jingsi, Gao, Xiaoyan, Shen, Yiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216800/
https://www.ncbi.nlm.nih.gov/pubmed/32160656
http://dx.doi.org/10.1002/mgg3.1212

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216800/
https://www.ncbi.nlm.nih.gov/pubmed/32160656
http://dx.doi.org/10.1002/mgg3.1212

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