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A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance

✍ Scribed by ROMINA ROMANIELLO; ALESSANDRA TONELLI; FILIPPO ARRIGONI; CINZIA BASCHIROTTO; FABIO TRIULZI; NEREO BRESOLIN; MARIA TERESA BASSI; RENATO BORGATTI


Book ID
115266857
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
249 KB
Volume
54
Category
Article
ISSN
0012-1622

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