✦ LIBER ✦
Identification of one novel causative mutation in exon 4 of WFS1 gene in two Italian siblings with classical DIDMOAD syndrome phenotype
✍ Scribed by Rigoli, Luciana; Lombardo, Fortunato; Salzano, Giuseppina; Di Bella, Chiara; Messina, Maria Francesca; De Luca, Filippo; Iafusco, Dario
- Book ID
- 122079067
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 372 KB
- Volume
- 526
- Category
- Article
- ISSN
- 0378-1119
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