☆ 4.5 Article

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

JOURNAL OF MEDICAL GENETICS (2003)

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Journal

JOURNAL OF MEDICAL GENETICS
Volume 40, Issue 9, Pages 709-713

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B M J PUBLISHING GROUP
DOI: 10.1136/jmg.40.9.709

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Genetics & Heredity

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