about
Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear DefectsDevelopment and clinical utility of a novel diagnostic nystagmus gene panel using targeted next-generation sequencing.Abnormal retinal development associated with FRMD7 mutations.Optic Nerve Head Development in Healthy Infants and Children Using Handheld Spectral-Domain Optical Coherence Tomography.Potential of handheld optical coherence tomography to determine cause of infantile nystagmus in children by using foveal morphology.In Vivo Foveal Development Using Optical Coherence Tomography.Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin EffectReading strategies in infantile nystagmus syndromeHomozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmusThe treatment of amblyopia: current practice and emerging trendsCongenital monocular elevation deficiency associated with a novel TUBB3 gene variantFRMD7-Related Infantile Nystagmus
P50
Q28116953-383ADD17-E414-4D3F-95BC-DB4172E13A00Q33815234-E26CD5B4-BA91-4241-BC98-D86ADC716F32Q33847626-E5D8A6D3-7CC7-4A3E-8890-4E7B707AC2ECQ37284172-1082CE40-ED26-4F19-AB99-7BE5ECEAD7F8Q45857507-BF5F3026-3EC1-468B-8A1F-3B7065E3A123Q50576613-F4C66A88-CEB1-4E22-B416-4D1162C45121Q57172473-BA1AB4B7-D7CC-4DEA-A27E-9D5540185AEFQ84813163-2054112F-FB13-44E4-9CF6-C6DAA1F28A7DQ90140001-0A352692-CD67-4FDC-AD80-F5769B2E4316Q91299538-E2B207FD-CCAE-4B8B-BA37-0E5414354B6EQ91856412-7A7EBF90-5287-4CF6-B77B-3B09612CE328Q94995185-F84C37A8-9954-40F3-A014-3AF2AD9EC077
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Gail Maconachie
@en
Gail Maconachie
@nl
type
label
Gail Maconachie
@en
Gail Maconachie
@nl
prefLabel
Gail Maconachie
@en
Gail Maconachie
@nl
P31
P496
0000-0001-9131-3480