Mitochondrial mutation associated with nonsyndromic deafness
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology
Reference28 articles.
1. Identification of mutations in the COL4A5 collagen gene in Alport syndrome;Barker;Science,1990
2. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene;Tassabehji;Nature,1992
3. The gene for an inherited form of deafness maps to chromosome 5831;Leon,1992
4. A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome;Robinson;Hum Genet,1992
5. A nonsyndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q;Guilford;Nat Genet,1994
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