A novel poreregion mutation, c. 887G> A (p. G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2

. (2017). A novel poreregion mutation, c. 887G> A (p. G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2. BMC MEDICAL GENETICS, 18(1), 36-36. SID. https://sid.ir/paper/719738/en

. A novel poreregion mutation, c. 887G> A (p. G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2. BMC MEDICAL GENETICS[Internet]. 2017;18(1):36-36. Available from: https://sid.ir/paper/719738/en

, “A novel poreregion mutation, c. 887G> A (p. G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2,” BMC MEDICAL GENETICS, vol. 18, no. 1, pp. 36–36, 2017, [Online]. Available: https://sid.ir/paper/719738/en