Clinical Characteristics of Three Cases with SAMD9/SAMD9L Gene Mutations
Mutations in the SAMD9 and SAMD9L genes are associated with MIRAGE syndrome and ATXPC syndrome, respectively. This study reports the clinical characteristics and genetic analysis of one case with SAMD9 mutation (c.3809T > A, p.F1270Y) and two cases with SAMD9L mutations (c.2675T > G, p.M892R;...
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Main Authors: | , , , , , , , |
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Format: | Article |
Language: | zho |
Published: |
Editorial Office of Journal of Rare Diseases
2024-10-01
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Series: | 罕见病研究 |
Subjects: | |
Online Access: | https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2024.04.014 |
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