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 (Q33970491)
scientific article published on August 1, 1992
Language:
Current Data About 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
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https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1379413/pdf/?tool=EBI
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https://europepmc.org/articles/PMC1682672
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https://europepmc.org/articles/PMC1682672?pdf=render
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(P1476) "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" (language: en)
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(P2093) McIntosh I
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A. Hamosh
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T. M. King
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B. J. Rosenstein
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M. Corey
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H. Levison
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P. Durie
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L. C. Tsui
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I. McIntosh
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M. Keston
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D. J. Brock
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other details
description scientific article published on August 1, 1992

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