Cite
HARVARD Citation
Liaqat, K. et al. (2018). Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. Journal of human genetics. 63 (11), pp. 1099-1107. [Online].
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Liaqat, K. et al. (2018). Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. Journal of human genetics. 63 (11), pp. 1099-1107. [Online].