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Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients

✍ Scribed by Kenji Asamura; Satoko Abe; Hisakuni Fukuoka; Yusuke Nakamura; Shin-ichi Usami

Book ID
116223202
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
247 KB
Volume
32
Category
Article
ISSN
0385-8146

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πŸ“œ SIMILAR VOLUMES

Lack of correlation between the type of
Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients
✍ Heini Hartikka; Kaija Kuurila; Jarmo KΓΆrkkΓΆ; Ilkka Kaitila; Reidar GrΓ©nman; Sepp πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 163 KB

## Communicated by Peter Byers Osteogenesis imperfecta (OI) is caused by mutations in COL1A1 and COL1A2 that code for the a1 and a2 chains of type I collagen. Phenotypes correlate with the mutation types in that COL1A1 null mutations lead to OI type I, and structural mutations in a1(I) or a2(I) lea

Lack of correlation between the type of
Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients
✍ Heini Hartikka; Kaija Kuurila; Jarmo KΓΆrkkΓΆ; Ilkka Kaitila; Reidar GrΓ©nman; Sepp πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 58 KB

The original article to which this Erratum refers was published in Human Mutation 24: 147-154 (2004). In Table 1 of the published original article, the fourth mutation should be c.913G4C (not c.913G4A as originally printed) and it should be bolded as it is a novel mutation. In addition, the last mu