Your search returned 3 results.

Results
	1.	Novel mutations in the CDKL5 gene in complex genotypes associated with West syndrome with variable phenotype: First description of somatic mosaic state. [electronic resource] by Jdila, Marwa Ben Issa, Abir Ben Khabou, Boudour Rhouma, Bochra Ben Kamoun, Fatma Ammar-Keskes, Leila Triki, Chahnez Fakhfakh, Faiza Producer: 20180507 In: Clinica chimica acta; international journal of clinical chemistry vol. 473 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Clinical, Molecular, and Computational Analysis Showed a Novel Homozygous Mutation Among the Substrate-Binding Site of ARSA Protein in Consanguineous Family with Late-Infantile MLD. [electronic resource] by Issa, Abir Ben Feki, Fatma Kammoun Jdila, Marwa Ben Khabou, Boudour Rhouma, Bochra Ben Ammar-Keskes, Leila Triki, Chahnez Fakhfakh, Faiza Producer: 20181109 In: Journal of molecular neuroscience : MN vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel C-terminal truncated mutation in hCDKL5 protein causing a severe West syndrome: Comparison with previous truncated mutations and genotype/phenotype correlation. [electronic resource] by Jdila, Marwa Ben Triki, Chahnez Rhouma, Bochra Ben Jomaa, Rihab Ben Issa, Abir Ben Ammar-Keskes, Leila Kamoun, Fatma Fakhfakh, Faiza Producer: 20190403 In: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)