“…15 This may not come as a surprise, as the POAG phenotype itself seems complex and to result from diverse pathological processes that involve, but are not limited to, the retina and optic nerve, the aqueous humor outflow pathways and even, as suggested recently, the cerebrospinal fluid dynamics. 16 In 2000, Wiggs et al 17 published a first genome-wide linkage scan involving an initial set of 41 multiplex families and a second one of 33, where several loci, including regions on chromosome 2, 14, 17 and 19, were linked to POAG. We, therefore, focused our efforts on chromosomal region 14q11.…”