Atıf İçin Kopyala
YUCEL G., YUCEL I., BAGCI H., AKSU G., LULECI G., GUMUSLU S., ...Daha Fazla
JAPANESE JOURNAL OF OPHTHALMOLOGY, cilt.36, sa.1, ss.33-36, 1992 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
36
Sayı:
1
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Basım Tarihi:
1992
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Dergi Adı:
JAPANESE JOURNAL OF OPHTHALMOLOGY
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.33-36
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Anahtar Kelimeler:
CONGENITAL COLOR BLINDNESS, GLUCOSE-6-PHOSPHATE DEHYDROGENASE, X-CHROMOSOME
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Akdeniz Üniversitesi Adresli:
Hayır
Özet
No erythrocyte glucose-6-phosphate dehydrogenase (G6PD)-deficient person was detected among 90 male patients with congenital color blindness (CCB) diagnosed at the Ophthalmology Clinic of our Hospital. Eighteen complete G6PD-deficient subjects had normal color vision. These results suggest that there is a linkage disequilibrium between CCB and G6PD genes.