@article {163,
	title = {New Arab family with cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome suggests a possible founder effect for the c.223delG mutation.},
	journal = {J Dermatol},
	volume = {42},
	year = {2015},
	month = {2015 Aug},
	pages = {821-2},
	keywords = {Arabs, Female, Founder Effect, Humans, Infant, Newborn, Keratoderma, Palmoplantar, Neurocutaneous Syndromes, Qb-SNARE Proteins, Qc-SNARE Proteins},
	issn = {1346-8138},
	doi = {10.1111/1346-8138.12917},
	author = {Ben-Salem, Salma and Nara, Sobreira and Al-Shamsi, Aisha M and Valle, David and Ali, Bassam R and Al-Gazali, Lihadh}
}
