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The impact of Congenital Long QT Syndrome on First Nations children and youth in...
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Genotype–phenotype correlations in CPT1A deficiency detected by newborn screenin...
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Utility of Genetic Testing for Confirmation of Abnormal Newborn Screening in Dis...
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The distribution of three candidate cold-resistant SNPs in six minorities in Nor...
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Carnitine Palmitoyl Transferase, Type 1A (CPT1A): The Arctic Variant
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3
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Author
Bene Watts, Simona
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Callum Wilson
1
Can Ficicioglu
1
Detlef Knoll
1
Dianne Webster
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Emma Glamuzina
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Isaac Bernhardt
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Jie Wu
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Kevin Carpenter
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Kexian Dong
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Lauren Lulis
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Leah Dowsett
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Leah K. Dowsett
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Lidan Xu
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Michael J. Bennett
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Michelle Maeda
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Patson, Amber Lee Madrid
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Qiuyan Li
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Sanmati Cuddapah
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Songbin Fu
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Wenjing Sun
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Xuelong Zhang
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Xueyuan Jia
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Topic
CPT1A
Genetics
2
QH426-470
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fatty acid oxidation disorders
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Arctic Variant
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Ashkenazi Jewish
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Biotechnology
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Diseases of the endocrine glands. Clinical endocrinology
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FADS
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First Nations
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Gitxsan
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LQTS
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Minorities
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North China
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RC648-665
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SNP
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TP248.13-248.65
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carnitine palmitoyltransferase 1A
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carnitine palmitoyltransferase deficiency
1
carnitine palmitoyltransferase type 1 deficiency
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children
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elevated liver transaminases
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long QT syndrome
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mitochondrial fatty acid oxidation
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neonatal screening
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newborn screening
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pediatric health
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pediatrics
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well-being
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youth
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Directory of Open Access Journals: DOAJ Articles
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Anesthesia eJournal - AEJ
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MDPI Open Access Publishing
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University of Victoria (Canada): UVicDSpace
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Arctic
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Greenland
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New Zealand
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English
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inuit
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Arctic
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Alaska
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Climate change
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Ewenki
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First Nations
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Greenland
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Inupiat
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Siberian Yupik
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Yupik
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