DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Tajima T, Hattorri T, Nakajima T , et al.
Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient.
J Clin Endocrinol Metab 2003;
88 (1) 45-50
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