Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?
- DOI
- 10.1002/humu.10130
- Published
- 2002 Oct
- Container
- Human mutation
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/humu.10130,
title = {Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?},
author = {Winnepenninckx B and Errijgers V and Hayez-Delatte F and Reyniers E and Frank Kooy R},
year = {2002},
journal = {Human mutation},
doi = {10.1002/humu.10130},
url = {https://doi.org/10.1002/humu.10130}
}RIS
TY - JOUR TI - Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening? AU - Winnepenninckx B AU - Errijgers V AU - Hayez-Delatte F AU - Reyniers E AU - Frank Kooy R PY - 2002 JO - Human mutation DO - 10.1002/humu.10130 UR - https://doi.org/10.1002/humu.10130 ER -
APA
B, W., V, E., F, H., E, R., & R, F. K. (2002). Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?. Human mutation. https://doi.org/10.1002/humu.10130
Source records
- pubmed · retrieved 2026-09-26T00:06:02.025Z