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Challenges in Clinicogenetic Correlations: One Gene – Many Phenotypes
BACKGROUND: Progress in genetics – particularly the advent of next‐generation sequencing (NGS) – has enabled an unparalleled gene discovery and revealed unmatched complexity of genotype–phenotype correlations in movement disorders. Among other things, it has emerged that mutations in one and the sam...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Mov Disord Clin Pract |
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| Κύριοι συγγραφείς: | , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
John Wiley & Sons, Inc.
2021
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8015894/ https://ncbi.nlm.nih.gov/pubmed/33816657 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.13165 |
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