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Year | Number of Results |
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2002 | 1 |
2003 | 2 |
2023 | 0 |
PubMed (OMIM) for id: 375052
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Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss.
Am J Hum Genet. 2003 Jun;72(6):1571-7. doi: 10.1086/375654. Epub 2003 May 6.
Am J Hum Genet. 2003.
PMID: 12736868
Free PMC article.
A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian family.
D'Adamo P, Pinna M, Capobianco S, Cesarani A, D'Eustacchio A, Fogu P, Carella M, Seri M, Gasparini P.
D'Adamo P, et al.
Hum Genet. 2003 Mar;112(3):319-20. doi: 10.1007/s00439-002-0880-6. Epub 2002 Dec 13.
Hum Genet. 2003.
PMID: 12596055
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