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Leber’s hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the ND4 gene and spontaneous recovery

✍ Scribed by Beate Leo-Kottler, Janina Luberichs, Dorothea Besch, Margot Christ-Adler, Sascha Fauser


Book ID
113040588
Publisher
Springer-Verlag
Year
2002
Tongue
English
Weight
252 KB
Volume
240
Category
Article
ISSN
0065-6100

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