Nitrogen Permease Regulator Like-2 (NPRL2) truncating mutation causes Ohtahara syndrome with incomplete penetrance: expanding the genotype-phenotype correlations-MedSci.cn - 梅斯（MedSci）

Nitrogen Permease Regulator Like-2 (NPRL2) truncating mutation causes Ohtahara syndrome with incomplete penetrance: expanding the genotype-phenotype correlations

Zhou, X; Chen, FY; Ye, XG; Liu, ZG

Liu, ZG (通讯作者)，Southern Med Univ, Affiliated Foshan Matern & Child Healthcare Hosp, Dept Pediat, 11 Renminxi Rd, Foshan 528000, Guangdong, Peoples R China.

CLINICAL DYSMORPHOLOGY, 2022; 31 (4): 181

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