Further evidence to link CHD family-chromatin remodeler genes and neurodevelopment: de novo variants in CHD5 are associated with intellectual disability, epilepsy and autism
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Lehalle, D; Mizuguchi, T; Nava, C; Matsumoto, N; Cope, H; de Man, S; Friedman, J; Joset, P; Kato, M; Muffels, I; Nakamura, K; Person, RE ...
Published in: EUROPEAN JOURNAL OF HUMAN GENETICS
2020
Duke Scholars
Published In
EUROPEAN JOURNAL OF HUMAN GENETICS
EISSN
1476-5438
ISSN
1018-4813
Publication Date
2020
Volume
28
Issue
SUPPL 1
Start / End Page
326 / 327
Related Subject Headings
- Genetics & Heredity
- 3202 Clinical sciences
- 3105 Genetics
- 1103 Clinical Sciences
- 0604 Genetics
Citation
APA
Chicago
ICMJE
MLA
NLM
Lehalle, D., Mizuguchi, T., Nava, C., Matsumoto, N., Cope, H., de Man, S., … Mignot, C. (2020). Further evidence to link CHD family-chromatin remodeler genes and neurodevelopment: de novo variants in CHD5 are associated with intellectual disability, epilepsy and autism. In EUROPEAN JOURNAL OF HUMAN GENETICS (Vol. 28, pp. 326–327).
Lehalle, D., T. Mizuguchi, C. Nava, N. Matsumoto, H. Cope, S. de Man, J. Friedman, et al. “Further evidence to link CHD family-chromatin remodeler genes and neurodevelopment: de novo variants in CHD5 are associated with intellectual disability, epilepsy and autism.” In EUROPEAN JOURNAL OF HUMAN GENETICS, 28:326–27, 2020.
Lehalle D, Mizuguchi T, Nava C, Matsumoto N, Cope H, de Man S, et al. Further evidence to link CHD family-chromatin remodeler genes and neurodevelopment: de novo variants in CHD5 are associated with intellectual disability, epilepsy and autism. In: EUROPEAN JOURNAL OF HUMAN GENETICS. 2020. p. 326–7.
Lehalle, D., et al. “Further evidence to link CHD family-chromatin remodeler genes and neurodevelopment: de novo variants in CHD5 are associated with intellectual disability, epilepsy and autism.” EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 28, no. SUPPL 1, 2020, pp. 326–27.
Lehalle D, Mizuguchi T, Nava C, Matsumoto N, Cope H, de Man S, Friedman J, Joset P, Kato M, Muffels I, Nakamura K, Person RE, Petit F, Rauch A, Shashi V, Smol T, Steindl K, Torti E, Van de Laar I, Fuchs S, Depienne C, Mignot C. Further evidence to link CHD family-chromatin remodeler genes and neurodevelopment: de novo variants in CHD5 are associated with intellectual disability, epilepsy and autism. EUROPEAN JOURNAL OF HUMAN GENETICS. 2020. p. 326–327.
Published In
EUROPEAN JOURNAL OF HUMAN GENETICS
EISSN
1476-5438
ISSN
1018-4813
Publication Date
2020
Volume
28
Issue
SUPPL 1
Start / End Page
326 / 327
Related Subject Headings
- Genetics & Heredity
- 3202 Clinical sciences
- 3105 Genetics
- 1103 Clinical Sciences
- 0604 Genetics