(PDF) A De Novo Missense Mutation in a Critical Domain of

A De Novo Missense Mutation in a Critical Domain of the X-Linked DDP Gene Causes the Typical Deafness–dystonia–optic Atrophy Syndrome

European Journal of Human Genetics - United Kingdom

doi 10.1038/sj.ejhg.5200483

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Date

June 1, 2000

Authors

Lisbeth Tranebjærg

Fons JM Gabreels

Marijke Van Ghelue

Publisher

Springer Science and Business Media LLC

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