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APA Citation
Rips, J., Almashanu, S., Mandel, H., Josephsberg, S., Lerman‐Sagie, T., Zerem, A., Podeh, B., Anikster, Y., Shaag, A., Luder, A., Staretz Chacham, O., & Spiegel, R. (2016). primary and maternal 3‐methylcrotonyl‐CoA carboxylase deficiency: insights from the Israel newborn screening program. Journal of inherited metabolic disease, 39(2), 211–217. http://access.bl.uk/ark:/81055/vdc_100079068027.0x000048