Cite
HARVARD Citation
Lerat, J. et al. (2017). A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature. Journal of the peripheral nervous system. 22 (2), pp. 77-84. [Online].
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Lerat, J. et al. (2017). A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature. Journal of the peripheral nervous system. 22 (2), pp. 77-84. [Online].