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Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects.

(2000) HUMAN MUTATION. 15(6). p.541-555
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Chicago
Messiaen, Ludwine, T CALLENS, Geert Mortier, DIANE BEYSEN, Ina Vandenbroucke, Nadine Van Roy, Franki Speleman, and Anne De Paepe. 2000. “Exhaustive Mutation Analysis of the NF1 Gene Allows Identification of 95% of Mutations and Reveals a High Frequency of Unusual Splicing Defects.” Human Mutation 15 (6): 541–555.
APA
Messiaen, L., CALLENS, T., Mortier, G., BEYSEN, D., Vandenbroucke, I., Van Roy, N., Speleman, F., et al. (2000). Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects. HUMAN MUTATION, 15(6), 541–555.
Vancouver
1.
Messiaen L, CALLENS T, Mortier G, BEYSEN D, Vandenbroucke I, Van Roy N, et al. Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects. HUMAN MUTATION. 2000;15(6):541–55.
MLA
Messiaen, Ludwine, T CALLENS, Geert Mortier, et al. “Exhaustive Mutation Analysis of the NF1 Gene Allows Identification of 95% of Mutations and Reveals a High Frequency of Unusual Splicing Defects.” HUMAN MUTATION 15.6 (2000): 541–555. Print.
@article{126953,
  author       = {Messiaen, Ludwine and CALLENS, T and Mortier, Geert and BEYSEN, DIANE and Vandenbroucke, Ina and Van Roy, Nadine and Speleman, Franki and De Paepe, Anne},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  language     = {eng},
  number       = {6},
  pages        = {541--555},
  title        = {Exhaustive mutation analysis of the NF1 gene allows identification of 95\% of mutations and reveals a high frequency of unusual splicing defects.},
  volume       = {15},
  year         = {2000},
}

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