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Oxford University Press

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A low prevalence of MYH7 / MYBPC3 mutations among Familial Hypertrophic Cardiomyopathy patients in India

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Springer Publishing Company

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Retinitis pigmentosa-associated rhodopsin mutations in three membrane-located cysteine residues present three different biochemical phenotypes

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Carnitine Transporter OCTN2 Mutations in Systemic Primary Carnitine Deficiency: A Novel Arg169Gln Mutation and a Recurrent Arg282ter Mutation Associated with an Unconventional Splicing Abnormality

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Genetic diversity of MYH ₃ gene associated with growth and carcass traits in Chinese Qinchuan cattle

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