Distribution of the Mutations Causing GT in Iraqi-Jewish Patients
I-J1 is an 11-bp deletion in exon 12. I-J2 is an 11.2-kb deletion of exons 10 through 13 (see text).
In five of the patients, the genotype was inferred from the genotypes of their immediate relatives.
Two siblings that bear neither I-J1 nor I-J2 mutations.
ρ A patient lost from follow-up.
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