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Autosomal Recessive Primary Microcephaly Due to ASPM Mutations: an Update.

Pascaline Letard,Severine Drunat,Yoann Vial,Sarah Duerinckx,Anais Ernault,Daniel Amram,Stephanie Arpin,Marta Bertoli,Tiffany Busa,Berten Ceulemans,Julie Desir,Martine Doco-Fenzy,Siham Chafai Elalaoui,Koenraad Devriendt,Laurence Faivre,Christine Francannet,David Genevieve,Marion Gerard,Cyril Gitiaux,Sophie Julia,Sebastien Lebon,Toni Lubala,Michele Mathieu-Dramard,Helene Maurey,Julia Metreau,Sanaa Nasserereddine,Mathilde Nizon,Genevieve Pierquin,Nathalie Pouvreau,Clothilde Rivier-Ringenbach,Massimiliano Rossi,Elise Schaefer,Abdelaziz Sefiani,Sabine Sigaudy,Yves Sznajer,Yusuf Tunca,Sophie Guilmin Crepon,Corinne Alberti,Monique Elmaleh-Berges,Brigitte Benzacken,Bernd Wollnick,C. Geoffrey Woods,Anita Rauch,Marc Abramowicz,Vincent El Ghouzzi,Pierre Gressens,Alain Verloes,Sandrine Passemard

Human Mutation（2017）

Cited 68|Views39
Key words
ASPM,brain development,brain imaging,centrosome,intellectual disability,MCPH,primary microcephaly
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