Skip to content

Opening book details…

About this Biochemistry, Genetics and Molecular Biology article

Two novel mutations in XYLT2 cause spondyloocular syndrome by Taylan, Fulya; Yavaş Abalı, Zehra; Jäntti, Nina; Güneş, Nilay; Darendeliler, Feyza; Baş, Firdevs; Poyrazoğlu, Şükran; Tamçelik, Nevbahar; Tüysüz, Beyhan; Mäkitie, Outi is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Taylan, Fulya; Yavaş Abalı, Zehra; Jäntti, Nina; Güneş, Nilay; Darendeliler, Feyza; Baş, Firdevs; Poyrazoğlu, Şükran; Tamçelik, Nevbahar; Tüysüz, Beyhan; Mäkitie, Outi
Publisher
John Wiley and Sons; Wiley (John Wiley & Sons); Wiley-Liss Inc; Wiley (ISSN 1552-4825)
Published
2017
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)