A genetic marker of the ACKR1 gene is present in patients with Type II congenital smell loss who have type I hyposmia and hypogeusia.
A genetic marker of the ACKR1 gene is present in patients with Type II congenital smell loss who have type I hyposmia and hypogeusia. — المؤلف: Stateman, William A — American journal of otolaryngology 20170925
- المؤلف
- Stateman, William A
- النشر
- American journal of otolaryngology 20170925
- الوصف
- 484-489 p.
- الموضوعات
- Adolescent؛ Adult؛ Aged؛ Case-Control Studies؛ Child؛ Cohort Studies؛ Duffy Blood-Group System؛ Female