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Mutations in the Wolfram Syndrome Type 1 Gene (WFSI) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss
OBJECTIVE: To describe low-frequency sensorineural hearing loss (LFSNHL) inherited as a dominant trait in 3 families and in 1 sporadic case. DESIGN: Longitudinal clinical study from 1968 to 2001. SETTING: Tertiary care hospital; field studies conducted by molecular genetic research laboratory. PARTI...
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| Τόπος έκδοσης: | Arch Otolaryngol Head Neck Surg |
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| Κύριοι συγγραφείς: | , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2003
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6145174/ https://ncbi.nlm.nih.gov/pubmed/12707187 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archotol.129.4.411 |
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