Mowat–Wilson syndrome: the clinical report with the novel mutation in ZFHX1B (exon 8: c.2372del C; p.T791fsX816)

Author: Sasso Antun   Paučić-Kirinčić Ela   Kamber-Makek Silvija   Sindičić Nada   Brajnović-Zaputović S.   Brajenović-Milić Bojana  

Publisher: Springer Publishing Company

ISSN: 0256-7040

Source: Child's Nervous System, Vol.24, Iss.5, 2008-05, pp. : 615-618

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