Information Journal Paper
APA:
Copy. (2018). Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. JOURNAL OF HUMAN GENETICS, 63(11), 1099-1107. SID. https://sid.ir/paper/719087/en
Vancouver:
Copy. Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. JOURNAL OF HUMAN GENETICS[Internet]. 2018;63(11):1099-1107. Available from: https://sid.ir/paper/719087/en
IEEE:
Copy, “Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment,” JOURNAL OF HUMAN GENETICS, vol. 63, no. 11, pp. 1099–1107, 2018, [Online]. Available: https://sid.ir/paper/719087/en