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Q36372871-B38492DE-B1E3-4894-9A63-6ADB585DCB58
Q36372871-B38492DE-B1E3-4894-9A63-6ADB585DCB58
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http://www.wikidata.org/entity/statement/Q36372871-B38492DE-B1E3-4894-9A63-6ADB585DCB58
Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.
P2860
Q36372871-B38492DE-B1E3-4894-9A63-6ADB585DCB58
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36372871-B38492DE-B1E3-4894-9A63-6ADB585DCB58
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wasDerivedFrom
ad0d3c052d9333c94823b0ff7ab7b2d3a2e41d44
P2860
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits