A de novo missense mutation in a critical domain of the...

European Journal of Human Genetics 2000 Vol. 8; Iss. 6

A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness–dystonia–optic atrophy syndrome

Tranebjærg, Lisbeth, Hamel, Ben CJ, Gabreels, Fons JM, Renier, Willy O, Ghelue, Marijke Van
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Volume:
8
Year:
2000
Language:
english
Pages:
4
DOI:
10.1038/sj.ejhg.5200483
File:
PDF, 164 KB
english, 2000
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