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A novel COLIA1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders
- Gensure, RC (author)
-
- Makitie, O (author)
- Karolinska Institutet
- Barclay, C (author)
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- Chan, C (author)
- DePalmer, S (author)
- Bastepe, M (author)
- Abuzahra, H (author)
- Couper, R (author)
- Seidman, J (author)
- Cole, WG (author)
- Juppner, H (author)
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- (creator_code:org_t)
- 2005
- 2005
- English.
- In: JOURNAL OF INVESTIGATIVE MEDICINE. - 1081-5589. ; 53:1, s. S272-S272
- Conference paper (other academic/artistic)
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- kon (subject category)
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- Gensure, RC
- Makitie, O
- Barclay, C
- Chan, C
- DePalmer, S
- Bastepe, M
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- Abuzahra, H
- Couper, R
- Seidman, J
- Cole, WG
- Juppner, H
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