Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome

M. Vivero, M. T. Cho, A. Begtrup, I. M. Wentzensen, Larry Walsh, K. Payne, Y. A. Zarate, K. Bosanko, G. B. Schaefer, S. Debrosse, L. Pollack, K. Mason, K. Retterer, S. Deward, J. Juusola, W. K. Chung

Research output: Contribution to journalArticle

4 Citations (Scopus)
Original languageEnglish (US)
JournalClinical Genetics
DOIs
StateAccepted/In press - 2017

Keywords

  • CLIFAHDD syndrome
  • de novo
  • NALCN
  • Neurodevelopmental disorder
  • Whole-exome sequencing

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Vivero, M., Cho, M. T., Begtrup, A., Wentzensen, I. M., Walsh, L., Payne, K., ... Chung, W. K. (Accepted/In press). Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome. Clinical Genetics. https://doi.org/10.1111/cge.12899

Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome. / Vivero, M.; Cho, M. T.; Begtrup, A.; Wentzensen, I. M.; Walsh, Larry; Payne, K.; Zarate, Y. A.; Bosanko, K.; Schaefer, G. B.; Debrosse, S.; Pollack, L.; Mason, K.; Retterer, K.; Deward, S.; Juusola, J.; Chung, W. K.

In: Clinical Genetics, 2017.

Research output: Contribution to journalArticle

Vivero, M, Cho, MT, Begtrup, A, Wentzensen, IM, Walsh, L, Payne, K, Zarate, YA, Bosanko, K, Schaefer, GB, Debrosse, S, Pollack, L, Mason, K, Retterer, K, Deward, S, Juusola, J & Chung, WK 2017, 'Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome', Clinical Genetics. https://doi.org/10.1111/cge.12899
Vivero, M. ; Cho, M. T. ; Begtrup, A. ; Wentzensen, I. M. ; Walsh, Larry ; Payne, K. ; Zarate, Y. A. ; Bosanko, K. ; Schaefer, G. B. ; Debrosse, S. ; Pollack, L. ; Mason, K. ; Retterer, K. ; Deward, S. ; Juusola, J. ; Chung, W. K. / Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome. In: Clinical Genetics. 2017.
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keywords = "CLIFAHDD syndrome, de novo, NALCN, Neurodevelopmental disorder, Whole-exome sequencing",
author = "M. Vivero and Cho, {M. T.} and A. Begtrup and Wentzensen, {I. M.} and Larry Walsh and K. Payne and Zarate, {Y. A.} and K. Bosanko and Schaefer, {G. B.} and S. Debrosse and L. Pollack and K. Mason and K. Retterer and S. Deward and J. Juusola and Chung, {W. K.}",
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AU - Cho, M. T.

AU - Begtrup, A.

AU - Wentzensen, I. M.

AU - Walsh, Larry

AU - Payne, K.

AU - Zarate, Y. A.

AU - Bosanko, K.

AU - Schaefer, G. B.

AU - Debrosse, S.

AU - Pollack, L.

AU - Mason, K.

AU - Retterer, K.

AU - Deward, S.

AU - Juusola, J.

AU - Chung, W. K.

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KW - Neurodevelopmental disorder

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