Coursimault, J., Guerrot, A.-M., Morrow, M. M., Schramm, C., Zamora, F. M., Shanmugham, A., Liu, S., Zou, F., Bilan, F., Le Guyader, G., Bruel, A.-L., Denommé-Pichon, A.-S., Faivre, L., Tran Mau-Them, F., Tessarech, M., Colin, E., El Chehadeh, S., Gérard, B., Schaefer, E., … Lecoquierre, F. (2021). MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects. Human Genetics, 141(1), 65–80. https://doi.org/10.1007/s00439-021-02383-z
Subjects:
Genetic Variation
(MeSH)
Nerve Tissue Proteins
(MeSH)
Neurodevelopmental Disorders
(MeSH)
Transcription Factors
(MeSH)
Publication Type:
Article
Unique ID:
10.1007/s00439-021-02383-z
PMID:
Journal:
Publication Date:
Data Source:
Scopus
Source Link: