Liu, Z., Zhang, L., Shen, D., Ding, C., Yang, X., Zhang, W., . . . Fang, F. (2019). Compound Heterozygous CHAT Gene Mutations of a Large Deletion and a Missense Variant in a Chinese Patient With Severe Congenital Myasthenic Syndrome With Episodic Apnea. Front Pharmacol.
Chicago Style citaatLiu, Zhimei, et al. "Compound Heterozygous CHAT Gene Mutations of a Large Deletion and a Missense Variant in a Chinese Patient With Severe Congenital Myasthenic Syndrome With Episodic Apnea." Front Pharmacol 2019.
MLA citatieLiu, Zhimei, et al. "Compound Heterozygous CHAT Gene Mutations of a Large Deletion and a Missense Variant in a Chinese Patient With Severe Congenital Myasthenic Syndrome With Episodic Apnea." Front Pharmacol 2019.
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