about
Development and clinical utility of a novel diagnostic nystagmus gene panel using targeted next-generation sequencing.The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusGender- and Ethnicity-Related Differences in Optic Nerve Head Topography in Healthy Indian and Caucasian Participants.The Role of FRMD7 in Idiopathic Infantile Nystagmus.A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus.Potential of handheld optical coherence tomography to determine cause of infantile nystagmus in children by using foveal morphology.Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia.Localization of Neurensin1 in cerebellar Purkinje cells of the developing chick and its possible function in dendrite formation.High-resolution in vivo imaging in achromatopsia.Is high-resolution spectral domain optical coherence tomography reliable in nystagmus?The functional significance of foveal abnormalities in albinism measured using spectral-domain optical coherence tomographyReading strategies in infantile nystagmus syndromeCongenital monocular elevation deficiency associated with a novel TUBB3 gene variant
P50
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P50
description
researcher ORCID: 0000-0002-4630-1234
@en
name
Mervyn Thomas
@ast
Mervyn Thomas
@en
Mervyn Thomas
@es
Mervyn Thomas
@nl
Mervyn Thomas
@sl
type
label
Mervyn Thomas
@ast
Mervyn Thomas
@en
Mervyn Thomas
@es
Mervyn Thomas
@nl
Mervyn Thomas
@sl
prefLabel
Mervyn Thomas
@ast
Mervyn Thomas
@en
Mervyn Thomas
@es
Mervyn Thomas
@nl
Mervyn Thomas
@sl
P106
P1153
55472021700
P21
P31
P496
0000-0002-4630-1234
P569
2000-01-01T00:00:00Z