Fahimi, H., Behroozi, S., Noavar, S., & Parvini, F. (2021). A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss. BMC Med Genomics.
Chicago Style CitationFahimi, Hossein, Samira Behroozi, Sadaf Noavar, i Farshid Parvini. "A Novel Recessive PDZD7 Bi-allelic Mutation in an Iranian Family With Non-syndromic Hearing Loss." BMC Med Genomics 2021.
Cita MLAFahimi, Hossein, Samira Behroozi, Sadaf Noavar, i Farshid Parvini. "A Novel Recessive PDZD7 Bi-allelic Mutation in an Iranian Family With Non-syndromic Hearing Loss." BMC Med Genomics 2021.
Atenció: Aquestes cites poden no estar 100% correctes.