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. 2013 Aug 8;33(5):386–389. doi: 10.3343/alm.2013.33.5.386

Fig. 2.

Fig. 2

DNA sequence analysis of the SPTA1 gene. The patient and her baby carried a heterozygous missense mutation in exon 2 (c.121C>T; p.Arg41Trp) in the alpha 1 domain. Protein changes are indicated by red lettering.