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Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies

✍ Scribed by Kondo, Yukiko; Koshimizu, Eriko; Megarbane, Andre; Hamanoue, Haruka; Okada, Ippei; Nishiyama, Kiyomi; Kodera, Hirofumi; Miyatake, Satoko; Tsurusaki, Yoshinori; Nakashima, Mitsuko; Doi, Hiroshi; Miyake, Noriko; Saitsu, Hirotomo; Matsumoto, Naomichi

Book ID: 125486235
Publisher: John Wiley and Sons
Year: 2013
Tongue: English
Weight: 716 KB
Volume: 161
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.35983

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