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High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients.
BMC Genomics. 2022 Apr 1;23(1):252. doi: 10.1186/s12864-022-08466-z.
BMC Genomics. 2022.
PMID: 35365085
Free PMC article.
Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population.
Petrova NV, Marakhonov AV, Balinova NV, Abrukova AV, Konovalov FA, Kutsev SI, Zinchenko RA.
Petrova NV, et al. Among authors: balinova nv.
Genes (Basel). 2021 May 27;12(6):820. doi: 10.3390/genes12060820.
Genes (Basel). 2021.
PMID: 34071867
Free PMC article.
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