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Comment
. 2019 Jan;21(1):260.
doi: 10.1038/s41436-018-0041-5. Epub 2018 Jun 30.

Noonan syndrome associated with growth hormone deficiency with biallelic LZTR1 variants

Marilena Nakaguma  1 , Alexander A L Jorge  2 , Ivo J P Arnhold  3
Affiliations
Comment

Noonan syndrome associated with growth hormone deficiency with biallelic LZTR1 variants

Marilena Nakaguma et al. Genet Med. 2019 Jan.
No abstract available

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Comment in

  • Response to Nakaguma et al.
    Biesecker LG. Biesecker LG. Genet Med. 2019 Jan;21(1):261. doi: 10.1038/s41436-018-0042-4. Epub 2018 Jun 30. Genet Med. 2019. PMID: 29959389 No abstract available.

Comment on

  • Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants.
    Johnston JJ, van der Smagt JJ, Rosenfeld JA, Pagnamenta AT, Alswaid A, Baker EH, Blair E, Borck G, Brinkmann J, Craigen W, Dung VC, Emrick L, Everman DB, van Gassen KL, Gulsuner S, Harr MH, Jain M, Kuechler A, Leppig KA, McDonald-McGinn DM, Can NTB, Peleg A, Roeder ER, Rogers RC, Sagi-Dain L, Sapp JC, Schäffer AA, Schanze D, Stewart H, Taylor JC, Verbeek NE, Walkiewicz MA, Zackai EH, Zweier C; Members of the Undiagnosed Diseases Network; Zenker M, Lee B, Biesecker LG. Johnston JJ, et al. Genet Med. 2018 Oct;20(10):1175-1185. doi: 10.1038/gim.2017.249. Epub 2018 Feb 22. Genet Med. 2018. PMID: 29469822 Free PMC article.

References

    1. Johnston JJ, van der Smagt JJ, Rosenfeld JA, et al. Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants. Genet Med. 2018. https://doi.org/10.1038/gim.2017.249 .

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