Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.
Journal Article (Journal Article)
A correction has been published to this Article. The PDF and HTML have been updated accordingly.
Full Text
Duke Authors
Cited Authors
- Koczkowska, M; Callens, T; Gomes, A; Sharp, A; Chen, Y; Hicks, AD; Aylsworth, AS; Azizi, AA; Basel, DG; Bellus, G; Bird, LM; Blazo, MA; Burke, LW; Cannon, A; Collins, F; DeFilippo, C; Denayer, E; Digilio, MC; Dills, SK; Dosa, L; Greenwood, RS; Griffis, C; Gupta, P; Hachen, RK; Hernández-Chico, C; Janssens, S; Jones, KJ; Jordan, JT; Kannu, P; Korf, BR; Lewis, AM; Listernick, RH; Lonardo, F; Mahoney, MJ; Ojeda, MM; McDonald, MT; McDougall, C; Mendelsohn, N; Miller, DT; Mori, M; Oostenbrink, R; Perreault, S; Pierpont, ME; Piscopo, C; Pond, DA; Randolph, LM; Rauen, KA; Rednam, S; Rutledge, SL; Saletti, V; Schaefer, GB; Schorry, EK; Scott, DA; Shugar, A; Siqveland, E; Starr, LJ; Syed, A; Trapane, PL; Ullrich, NJ; Wakefield, EG; Walsh, LE; Wangler, MF; Zackai, E; Claes, KBM; Wimmer, K; van Minkelen, R; De Luca, A; Martin, Y; Legius, E; Messiaen, LM
Published Date
- March 2019
Published In
Volume / Issue
- 21 / 3
Start / End Page
- 764 - 765
PubMed ID
- 30275510
Pubmed Central ID
- PMC7608433
Electronic International Standard Serial Number (EISSN)
- 1530-0366
Digital Object Identifier (DOI)
- 10.1038/s41436-018-0326-8
Language
- eng
Conference Location
- United States