Found: 2
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Intermediate autosomal recessive osteopetrosis with a large noncoding deletion in SNX10: A case report.
- Published in:
- 2019
- By:
- Publication type:
- letter
Molecular and clinical descriptions of patients with GABA<sub>A</sub> receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2): A cohort study, review of literature, and genotype–phenotype correlation.
- Published in:
- Epilepsia (Series 4), 2022, v. 63, n. 10, p. 2519, doi. 10.1111/epi.17336
- By:
- Publication type:
- Article