Table 2.

Distribution of the Mutations Causing GT in Iraqi-Jewish Patients

Genotype*PatientsFamilies
I-J1/I-J1 31 16 
I-J2/I-J2 
I-J1/I-J2 
Undefined 
Not examinedρ 
Total 40 21 
Genotype*PatientsFamilies
I-J1/I-J1 31 16 
I-J2/I-J2 
I-J1/I-J2 
Undefined 
Not examinedρ 
Total 40 21 
*

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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