Molecular Genetic Analysis of Inherited Kidney Dysfunction
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https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000484.v1.p1
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Samples were chosen for sequencing from a set of probands from pedigrees with apparently inherited forms of focal segmental glomerulosclerosis (FSGS). Several genes have been identified which when mutated cause FSGS under both recessive and dominant inheritance patterns. These known genes are estimated to explain less than 50% of inherited FSGS. We chose samples from individuals in which previous analyses of known disease genes failed to identify likely disease-causing mutations.]]>
Inclusion - Cases: FSGS or steroid-resistant nephritic syndrome. Exclusion: Clear secondary causes of kidney disease. No age exclusions. ]]>
Ongoing since 1996.]]>
创建时间:
2012-04-26



