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A novel mutation in the gene encoding TIMM8a, a component of the mitochondrial protein translocase complexes, in a Spanish familial case of deafness-dystonia (Mohr–Tranebjaerg) syndrome

✍ Scribed by Luis A. Aguirre; Ignacio del Castillo; Alfons Macaya; Carme Medá; Manuela Villamar; Miguel A. Moreno-Pelayo; Felipe Moreno

Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 178 KB
Volume: 140A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.31079

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