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

✍ Scribed by Luis A. Aguirre; Manuel Pérez-Bas; Manuela Villamar; M. Asunción López-Ariztegui; Miguel A. Moreno-Pelayo; Felipe Moreno; Ignacio del Castillo

Book ID: 116793816
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 223 KB
Volume: 18
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2008.09.009

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