File:PMC2694638 jkms-22-998-g002.png

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PMC2694638_jkms-22-998-g002.png ‎(468 × 384 pixels, file size: 167 KB, MIME type: image/png)

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Summary

Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0) Author:Park SK, Kim CS, Song DK, Kim JY, Choi IJ, Kim DK, Department of Anatomy, School of Medicine, Keimyung University(Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC2694638_jkms-22-998-g002&query=&req=4 Description:F2: Sequencing identification of the missense mutation in exon 2 of the WAS gene. The asterisk (*) indicated a single base "G" to "A" substitution in the affected patient (C) compared with a normal control (A), causing replacement of arginine by histidine at the amino acid residue 86 (Arg86His). WAS exon 2 sequence in female heterozygotes (B).

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Date/TimeThumbnailDimensionsUserComment
current20:55, 13 February 2022Thumbnail for version as of 20:55, 13 February 2022468 × 384 (167 KB)Ozzie10aaaaAuthor:Park SK, Kim CS, Song DK, Kim JY, Choi IJ, Kim DK, Department of Anatomy, School of Medicine, Keimyung University(Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC2694638_jkms-22-998-g002&query=&req=4 Description:F2: Sequencing identification of the missense mutation in exon 2 of the WAS gene. The asterisk (*) indicated a single base "G" to "A" substitution in the affected patient (C) compared with a normal control (A), causing replacement of a...

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