Genetic Heterogeneity and Human Disease

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Genetic Heterogeneity in Human Disease

Strong evidence suggests that rare mutations of severe effect are responsible for a substantial portion of complex human disease. Evolutionary forces generate vast genetic heterogeneity in human illness by introducing many new variants in each generation. Current sequencing technologies offer the possibility of finding rare disease-causing mutations and the genes that harbor them.

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Genetic heterogeneity in Gaucher disease.

Considerable clinical variability occurs in adult Gaucher disease type I and three main subtypes may be delineated: a very mild form, a severe form, and a moderate form which itself presents various clinical manifestations. A study based on 25 families from our clinic and a review of published reports showed that when both parents were heterozygous and more than one child was affected with Gauc...

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Genetic heterogeneity in inherited disease.

During the last few years a quiet revolution has been taking place in our ideas about the genetical basis of inherited disease. One way in which this has been manifested is by the increasing use in the literature of the term 'genetic heterogeneity', a term which is usually meant to imply that the same or very similar clinical syndromes may be produced by a number of quite different gene mutatio...

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Genetic heterogeneity in Parkinson disease

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Genetic Heterogeneity in Algerian Human Populations

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ژورنال

عنوان ژورنال: European Journal of Human Genetics

سال: 2015

ISSN: 1018-4813,1476-5438

DOI: 10.1038/ejhg.2015.2