Identification of Novel Mutations in FAH Gene and Prenatal Diagnosis of Tyrosinemia in Indian Family

<table><i>FAH</i> gene sequencing study in heterozygous pregnancy (3rd gravida). (a) <i>FAH</i> gene sequencing study showing c.648C&gt;G (p.Ile216Met) mutation in exon 8. (b) <i>FAH</i> gene sequencing study showing c.1159G&gt;A (p.Gly387Arg) mutation in exon 13.</table>

Case Reports in Genetics

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Figure 2

Figure 2: Identification of Novel Mutations in FAH Gene and Prenatal Diagnosis of Tyrosinemia in Indian Family 