DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling

Schueler, M (author)

Braun, DA (author)

Chandrasekar, G (author)

Karolinska Institutet

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Gee, HY (author)

Klasson, TD (author)

Halbritter, J (author)

Bieder, A (author)

Karolinska Institutet

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, I (author)

Karolinska Institutet

Lifton, RP (author)

Giles, RH (author)

Kere, J (author)

Karolinska Institutet

Hildebrandt, F (author)

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 (creator_code:org_t)

Elsevier BV, 2015

2015

English.

In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 96:1, s. 81-92

Related links:

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• Journal article (peer-reviewed)