DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Karaca E, Buyukkaya R, Pehlivan D. , et al.
Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome.
J Clin Endocrinol Metab 2015;
100 (01) E140-E147
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