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Q34205956-57B587DC-2F87-4B06-BBD0-64C91009F7A2
Q34205956-57B587DC-2F87-4B06-BBD0-64C91009F7A2
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http://www.wikidata.org/entity/statement/Q34205956-57B587DC-2F87-4B06-BBD0-64C91009F7A2
Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis.
P2860
Q34205956-57B587DC-2F87-4B06-BBD0-64C91009F7A2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34205956-57B587DC-2F87-4B06-BBD0-64C91009F7A2
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wasDerivedFrom
34a329810b8f70a71fb39ed5d47c37699de10b54
P2860
Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus