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MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype
Smol, T., Petit, F., Piton, A., Keren, B., Sanlaville, D., Afenjar, A., Baker, S., Bedoukian, E. C., Bhoj, E. J., Bonneau, D., Boudry-Labis, E., Bouquillon, S., Boute-Benejean, O., Caumes, R., ChatronLanguage:
english
Journal:
neurogenetics
DOI:
10.1007/s10048-018-0541-0
Date:
March, 2018
File:
PDF, 7.33 MB
english, 2018