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Open Access

Peer-reviewed

Research Article

A Deletion in FOXN1 Is Associated with a Syndrome Characterized by Congenital Hypotrichosis and Short Life Expectancy in Birman Cats

Marie Abitbol ,

* E-mail: m.abitbol@vet-alfort.fr

Affiliations U955 IMRB, INSERM, Équipe 10, Créteil, France, BNMS—Génétique Médicale Comparée des Affections Neuromusculaires, École nationale vétérinaire d'Alfort, Maisons-Alfort, France
⨯
Philippe Bossé,

Affiliations U955 IMRB, INSERM, Équipe 10, Créteil, France, BNMS—Génétique Médicale Comparée des Affections Neuromusculaires, École nationale vétérinaire d'Alfort, Maisons-Alfort, France
⨯
Anne Thomas,

Affiliation Antagene, La Tour de Salvagny, France
⨯
Laurent Tiret

Affiliations U955 IMRB, INSERM, Équipe 10, Créteil, France, BNMS—Génétique Médicale Comparée des Affections Neuromusculaires, École nationale vétérinaire d'Alfort, Maisons-Alfort, France
⨯

A Deletion in FOXN1 Is Associated with a Syndrome Characterized by Congenital Hypotrichosis and Short Life Expectancy in Birman Cats

Marie Abitbol,
Philippe Bossé,
Anne Thomas,
Laurent Tiret

x

Published: March 17, 2015
https://doi.org/10.1371/journal.pone.0120668

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