These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Ala397Asp mutation of myosin VIIA gene segregating in a Spanish family with type-Ib Usher syndrome. Author: Espinós C, Millán JM, Sánchez F, Beneyto M, Nájera C. Journal: Hum Genet; 1998 Jun; 102(6):691-4. PubMed ID: 9703432. Abstract: In the current study, 12 Spanish families affected by type-I Usher syndrome, that was previously linked to chromosome 11q, were screened for the presence of mutations in the N-terminal coding portion of the motor domain of the myosin VIIA gene by single-strand conformation polymorphism analysis of the first 14 exons. A mutation (Ala397Asp) segregating with the disease was identified, and several polymorphisms were also detected. It is presumed that the other USHIB mutations in these families could be located in the unscreened regions of the gene.[Abstract] [Full Text] [Related] [New Search]