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HARVARD Citation
Roche, E. et al. (2018). A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome. Clinical endocrinology. pp. 813-823. [Online].
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Roche, E. et al. (2018). A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome. Clinical endocrinology. pp. 813-823. [Online].