Sökresultat - Eva Gak
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Novel FOXG1 mutations associated with the congenital variant of Rett syndrome av Maria Antonietta Mencarelli, Ariele Spanhol-Rosseto, Rosangela Artuso, Dalila Rondinella, Roberta De Filippis, Nadia Bahi‐Buisson, Juliette Nectoux, R. Rubinsztajn, Thierry Bienvenu, A. Moncla, B. Chabrol, Laurent Villard, Zita Krūmiņa, Judith Armstrong, Ana Roche, M. Pineda, Eva Gak, Francesca Mari, Francesca Ariani, Alessandra Renieri
Publicerad 2009Artigo
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Biology
Gene
Genetics
Medicine
Internal medicine
Mutation
Receptor
Rett syndrome
Allele
Atrial fibrillation
Biochemistry
Bioinformatics
Biological activity
Brain-derived neurotrophic factor
CYP2C9
Cell biology
Chemistry
Disulfide bond
Endocrinology
Enzyme
Gastroenterology
Genotype
Growth factor
Haplotype
Hepatocyte
Hepatocyte growth factor
In vitro
MECP2
Mutagenesis
Mutant