Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria

Author: Valence Stéphanie   Poirier Karine   Lebrun Nicolas   Saillour Yoann   Sonigo Pascale   Bessières Bettina   Attié-Bitach Tania   Benachi Alexandra   Masson Cécile   Encha-Razavi Ferechté   Chelly Jamel   Bahi-Buisson Nadia  

Publisher: Springer Publishing Company

ISSN: 1364-6745

Source: Neurogenetics, Vol.14, Iss.3-4, 2013-11, pp. : 215-224

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