A Pilot Study for the Prevalence of Methylenetetrahydrofolate Reductase Gene Mutation in Egyptian Children with Homocystinuria
Ghada Maher Thabet;
Abstract
Objective: To determine the prevalence of C677T MTHFR gene mutation among children suffering from homocystinuria and the severity of clinical manifestations.
Methods: 7 families (7 cases, 9 siblings and 12 parents) & 20 healthy age and sex matched subjec
Methods: 7 families (7 cases, 9 siblings and 12 parents) & 20 healthy age and sex matched subjec
Other data
| Title | A Pilot Study for the Prevalence of Methylenetetrahydrofolate Reductase Gene Mutation in Egyptian Children with Homocystinuria | Other Titles | دراسة مبدئية عن نسبة طفرات جين الميثلين تتراهيدروفولات ريدكتيز بين الاطفال المصريين المصابين بالهوموسيستانوريا | Authors | Ghada Maher Thabet | Keywords | A Pilot Study for the Prevalence of Methylenetetrahydrofolate Reductase Gene Mutation in Egyptian Children with Homocystinuria | Issue Date | 2009 | Description | Objective: To determine the prevalence of C677T MTHFR gene mutation among children suffering from homocystinuria and the severity of clinical manifestations. Methods: 7 families (7 cases, 9 siblings and 12 parents) & 20 healthy age and sex matched subjec |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 94150r1979.pdf | 135.22 kB | Adobe PDF | View/Open |
Similar Items from Core Recommender Database
Items in Ain Shams Scholar are protected by copyright, with all rights reserved, unless otherwise indicated.