Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.

Horn D, Kapeller J, Rivera-Brugués N, Moog U, Lorenz-Depiereux B, Eck S, Hempel M, Wagenstaller J, Gawthrope A, Monaco AP, Bonin M, Riess O, Wohlleber E, Illig T, Bezzina CR, Franke A, Spranger S, Villavicencio-Lorini P, Seifert W, Rosenfeld J, Klopocki E, Rappold GA, Strom TM

Open source

DOI
10.1002/humu.21362
Published
2010 Nov
Container
Human mutation
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1002/humu.21362,
  title = {Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.},
  author = {Horn D and Kapeller J and Rivera-Brugués N and Moog U and Lorenz-Depiereux B and Eck S and Hempel M and Wagenstaller J and Gawthrope A and Monaco AP and Bonin M and Riess O and Wohlleber E and Illig T and Bezzina CR and Franke A and Spranger S and Villavicencio-Lorini P and Seifert W and Rosenfeld J and Klopocki E and Rappold GA and Strom TM},
  year = {2010},
  journal = {Human mutation},
  doi = {10.1002/humu.21362},
  url = {https://doi.org/10.1002/humu.21362}
}

RIS

TY  - JOUR
TI  - Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
AU  - Horn D
AU  - Kapeller J
AU  - Rivera-Brugués N
AU  - Moog U
AU  - Lorenz-Depiereux B
AU  - Eck S
AU  - Hempel M
AU  - Wagenstaller J
AU  - Gawthrope A
AU  - Monaco AP
AU  - Bonin M
AU  - Riess O
AU  - Wohlleber E
AU  - Illig T
AU  - Bezzina CR
AU  - Franke A
AU  - Spranger S
AU  - Villavicencio-Lorini P
AU  - Seifert W
AU  - Rosenfeld J
AU  - Klopocki E
AU  - Rappold GA
AU  - Strom TM
PY  - 2010
JO  - Human mutation
DO  - 10.1002/humu.21362
UR  - https://doi.org/10.1002/humu.21362
ER  - 

APA

D, H., J, K., N, R., U, M., B, L., S, E., M, H., J, W., A, G., AP, M., M, B., O, R., E, W., T, I., CR, B., A, F., S, S., P, V., W, S., J, R., E, K., GA, R., & TM, S. (2010). Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.. Human mutation. https://doi.org/10.1002/humu.21362

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