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- Schueler, M (author)
DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling
- Article/chapterEnglish2015
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- Elsevier BV,2015
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:130593507
- http://kipublications.ki.se/Default.aspx?queryparsed=id:130593507URI
- https://doi.org/10.1016/j.ajhg.2014.12.002DOI
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- Language:English
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- Braun, DA (author)
- Chandrasekar, GKarolinska Institutet (author)
- Gee, HY (author)
- Klasson, TD (author)
- Halbritter, J (author)
- Bieder, AKarolinska Institutet (author)
- Porath, JD (author)
- Airik, R (author)
- Zhou, WB (author)
- LoTurco, JJ (author)
- Che, A (author)
- Otto, EA (author)
- Bockenhauer, D (author)
- Sebire, NJ (author)
- Honzik, T (author)
- Harris, PC (author)
- Koon, SJ (author)
- Gunay-Aygun, M (author)
- Saunier, S (author)
- Zerres, K (author)
- Bruechle, NO (author)
- Drenth, JPH (author)
- Pelletier, L (author)
- Tapia-Paez, IKarolinska Institutet (author)
- Lifton, RP (author)
- Giles, RH (author)
- Kere, JKarolinska Institutet (author)
- Hildebrandt, F (author)
- Karolinska Institutet (creator_code:org_t)
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- In:American journal of human genetics: Elsevier BV96:1, s. 81-921537-66050002-9297
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