Two novel mutations in XYLT2...

American Journal of Medical Genetics Part A 2017 / 09

Two novel mutations in XYLT2 cause spondyloocular syndrome

Taylan, Fulya, Yavaş Abalı, Zehra, Jäntti, Nina, Güneş, Nilay, Darendeliler, Feyza, Baş, Firdevs, Poyrazoğlu, Şükran, Tamçelik, Nevbahar, Tüysüz, Beyhan, Mäkitie, Outi
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Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.38470
Date:
September, 2017
File:
PDF, 685 KB
english, 2017
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