Human Genome Variation - Table of Contents alert Volume 2, February 2015

Table of Contents: February 2015 Brief Communication | 26 February 2015 Truncating mutation in NFIA causes brain malformation and urinary tract defects Yutaka Negishi, Fuyuki Miya, Ayako Hattori, Kentaro Mizuno, Ikumi Hori et al. Human Genome Variation 2, Article number: 15007 | doi:10.1038/hgv.2015.7 Review Article | 26 February 2015 The many faces of KIF7 Duna Barakeh, Eissa Faqeih, Shams Anazi, Mohammed S Al-Dosari, Ameen Softah et al. Human Genome Variation 2, Article number: 15006 | doi:10.1038/hgv.2015.6 Article | 12 February 2015 DGCR6 at the proximal part of the DiGeorge critical region is involved in conotruncal heart defects Wenming Gao, Takashi Higaki, Minenori Eguchi-Ishimae, Hidehiko Iwabuki, Zhouying Wu et al. Human Genome Variation 2, Article number: 15004 | doi:10.1038/hgv.2015.4 Brief Communication | 12 February 2015 Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome Ikuya Tsuge, Masashi Morishita, Takema Kato, Makiko Tsutsumi, Hidehito Inagaki et al. Human Genome Variation 2, Article number: 15003 | doi:10.1038/hgv.2015.3 Brief Communication | 12 February 2015 A FRMD7 variant in a Japanese family causes congenital nystagmus Tomohiro Kohmoto, Nana Okamoto, Shigeko Satomura, Takuya Naruto, Takahide Komori et al. Human Genome Variation 2, Article number: 15002 | doi:10.1038/hgv.2015.2