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Q35194533-E8DDFD0D-0CB6-4556-99FB-B0E6A17DAA78
Q35194533-E8DDFD0D-0CB6-4556-99FB-B0E6A17DAA78
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http://www.wikidata.org/entity/statement/Q35194533-E8DDFD0D-0CB6-4556-99FB-B0E6A17DAA78
Homologous recombination among three intragene Alu sequences causes an inversion-deletion resulting in the hereditary bleeding disorder Glanzmann thrombasthenia.
P2860
Q35194533-E8DDFD0D-0CB6-4556-99FB-B0E6A17DAA78
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35194533-E8DDFD0D-0CB6-4556-99FB-B0E6A17DAA78
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wasDerivedFrom
2e58da8d7f56e80e08f536ca06bbb6ac5c46effa
P2860
Exon-Alu recombination deletes 5 kilobases from the low density lipoprotein receptor gene, producing a null phenotype in familial hypercholesterolemia