Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia

Gordon, CT (author)

Weaver, KN (author)

Zechi-Ceide, RM (author)

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Madsen, EC (author)

Tavares, ALP (author)

Oufadem, M (author)

Kurihara, Y (author)

Adameyko, I (author)

Karolinska Institutet

Picard, A (author)

Breton, S (author)

Pierrot, S (author)

Biosse-Duplan, M (author)

Voisin, N (author)

Masson, C (author)

Bole-Feysot, C (author)

Nitschke, P (author)

Delrue, MA (author)

Lacombe, D (author)

Guion-Almeida, ML (author)

Moura, PP (author)

Garib, DG (author)

Munnich, A (author)

Ernfors, P (author)

Karolinska Institutet

Hufnagel, RB (author)

Hopkin, RJ (author)

Kurihara, H (author)

Saal, HM (author)

Weaver, DD (author)

Katsanis, N (author)

Lyonnet, S (author)

Golzio, C (author)

Clouthier, DE (author)

Amiel, J (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. ; 96:4, s. 519-531

Related links:

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https://doi.org/10.1...

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• Journal article (peer-reviewed)