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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
Author(s) -
Aguirre Luis A.,
del Castillo Ignacio,
Macaya Alfons,
Medá Carme,
Villamar Manuela,
MorenoPelayo Miguel A.,
Moreno Felipe
Publication year - 2006
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.31079
Subject(s) - humanities , medicine , philosophy
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