Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
Magini, Pamela, Smits, Daphne J., Vandervore, Laura, Schot, Rachel, Columbaro, Marta, Kasteleijn, Esmee, van der Ent, Mees, Palombo, Flavia, Lequin, Maarten H., Dremmen, Marjolein, de Wit, Marie ClairЖурнал:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2019.08.006
Date:
September, 2019
Файл:
PDF, 3.12 MB
2019
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