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Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation.
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- 2024
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- Correction Notice
Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-58452-6
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- Publication type:
- Article
Han family with essential tremor caused by the P421L variant of the TENM4 gene in China.
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- Neurological Sciences, 2023, v. 44, n. 6, p. 2003, doi. 10.1007/s10072-023-06603-4
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- Article
Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.
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- BioMed Research International, 2021, p. 1, doi. 10.1155/2021/9973161
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- Article
Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-58452-6
- By:
- Publication type:
- Article