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A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency

✍ Scribed by Macchiaroli, Annamaria; Kelberman, Daniel; Auriemma, Renata Simona; Drury, Suzanne; Islam, Lily; Giangiobbe, Sara; Ironi, Gabriele; Lench, Nicholas; Sowden, Jane C.; Colao, Annamaria; Pivonello, Rosario; Cavallo, Luciano; Gasperi, Maurizio; Faienza, Maria Felicia

Book ID: 121461620
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 466 KB
Volume: 534
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2013.10.043

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