2018
DOI: 10.1007/978-981-13-0884-0_5
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Inherited Ocular Disease in the New Zealand Māori: Novel Genetic Mechanisms and Founder Effects

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Cited by 1 publication
(2 citation statements)
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“…In a study of 159 patients with childhood‐onset retinal dystrophy 11 patients were Māori, with the most common ocular phenotype being a rod‐cone dystrophy 87 . Although many IRDs remain genetically uncharacterised particularly for Māori, it is important for clinicians to understand the population‐specific genetic disease spectrum, the clinical phenotypes, and have a knowledge of regional ancestry and iwi to aid the diagnosis of IRD 88 …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In a study of 159 patients with childhood‐onset retinal dystrophy 11 patients were Māori, with the most common ocular phenotype being a rod‐cone dystrophy 87 . Although many IRDs remain genetically uncharacterised particularly for Māori, it is important for clinicians to understand the population‐specific genetic disease spectrum, the clinical phenotypes, and have a knowledge of regional ancestry and iwi to aid the diagnosis of IRD 88 …”
Section: Resultsmentioning
confidence: 99%
“…87 Although many IRDs remain genetically uncharacterised particularly for M aori, it is important for clinicians to understand the population-specific genetic disease spectrum, the clinical phenotypes, and have a knowledge of regional ancestry and iwi to aid the diagnosis of IRD. 88…”
Section: Inherited Retinal Dystrophiesmentioning
confidence: 99%