Primary coenzyme Q10 Deficiency-6 (COQ10D6): Two siblings with variable expressivity of the renal phenotype

出版年份 2019 全文链接

标题

作者

关键词

COQ6, mutation, COQ8B, mutation, Nephrotic syndrome, SRNS, CoQ6, Sensorineural deafness

出版物

Volume -, Issue -, Pages -

出版商

Elsevier BV

发表日期

2019-01-24

DOI

10.1016/j.ejmg.2019.01.011

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