Fig. 1
From: Defining the molecular pathology and consequent phenotypes in Egyptian HB patients
Partial nucleotide sequence of F9 gene. a Missense mutation c.676C>G in exon 6 identified in patients no. 1 and 2. b Missense mutation c.1305T>G in exon 8 identified in patient no. 3. c Nonsense mutation c.880C>T in exon 8 identified in families no. 4, 5, 6. d Nonsense mutation c.1150C>T in exon 8 identified in carrier mother family no. 7 (W for wild and M for mutant)