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A:
A question was asked here but turned out to be a dup of a missing tag.
So, I took the liberty to just give the OP the correct answer, even if it turns out to be wrong.
xcodebuild build-for-testing -scheme ”WorldViewXClean” -configuration ”Debug” -archivePath ”path/to/new.xcarchive” -archivePath ”path/to/new.ipa” -destination ”iOS” -quiet
This will built the build for iOS devices with the scheme, configuration and specified deployment target. If you don’t want to use xcodebuild it should be possible with xcrun. See the man page and its manpage.
Parry-Romberg syndrome caused by a mutation in RECQL4 gene.
Parry-Romberg syndrome (PRS) is a rare, autosomal dominant hereditary disease with a wide variety of clinical manifestations. Mutations in the RECQL4 gene are a common cause of PRS. RecQ helicases are composed of a conserved core region and variable regions. In the vertebrate homologues of RECQL4, the variable region consists of the exonuclease domains and is sometimes referred to as the 5′-3′ helicase module. On the basis of the N- and C-terminal structure of the vertebrate homologues, the RECQL4 helicase has been classified as a member of the RecQ subfamily of helicases. In this study, we identified a previously uncharacterized missense mutation, T3384A, in the variable region of RECQL4 as a cause of PRS. T3384 is conserved in the vertebrate homologues, and it is located in the middle of the 5′-3′ helicase module. These observations suggest that the T3384A mutation may affect the enzymatic function of the 5′-3′ helicase module of RECQL4. This is the first report showing that the variable region of RecQ helicases is important for the function of the protein.DELETE FROM `script_texts` WHERE `entry` BETWEEN -1628943 AND -1628942;
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