A novel mutation in <i>CDSN</i> causes peeling skin disease in a patient from Morocco

A Missense Mutation in TGM5 Causes Acral Peeling Skin Syndrome in a Tunisian Family

A novel mutation in the <i>GARS</i> gene in a Malian family with Charcot‐Marie‐Tooth disease

Abstract Background Charcot‐Marie‐Tooth (CMT) disease is a very heterogeneous neurological condit

A novel <i>UBE3A</i> truncating mutation in large Tunisian Angelman syndrome pedigree

Abstract We identified in a large Tunisian pedigree a novel UBE3A frameshift mutation in exon 16 co

Mutation in sorghum <i>LOW GERMINATION STIMULANT 1</i> alters strigolactones and causes <i>Striga</i> resistance

Significance The parasitic weed Striga

A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family

International audience Deafness and myopia syndrome is characterized by moderate-prof

46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the &lt;b&gt;&lt;i&gt;HSD17B3&lt;/i&gt;&lt;/b&gt; Gene

In this study, we present a Sudanese 46,XY patient raised as a female and diagnosed at the age of 20