ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.

التفاصيل البيبلوغرافية
العنوان: ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.
المؤلفون: Carapito R, Ivanova EL, Morlon A, Meng L, Molitor A, Erdmann E, Kieffer B, Pichot A, Naegely L, Kolmer A, Paul N, Hanauer A, Tran Mau-Them F, Jean-Marçais N, Hiatt SM, Cooper GM, Tvrdik T, Muir AM, Dimartino C, Chopra M, Amiel J, Gordon CT, Dutreux F, Garde A, Thauvin-Robinet C, Wang X, Leduc MS, Phillips M, Crawford HP, Kukolich MK, Hunt D, Harrison V, Kharbanda M, Smigiel R, Gold N, Hung CY, Viskochil DH, Dugan SL, Bayrak-Toydemir P, Joly-Helas G, Guerrot AM, Schluth-Bolard C, Rio M, Wentzensen IM, McWalter K, Schnur RE, Lewis AM, Lalani SR, Mensah-Bonsu N, Céraline J, Sun Z, Ploski R, Bacino CA, Mefford HC, Faivre L, Bodamer O, Chelly J, Isidor B, Bahram S
مؤلفون مشاركون: Deciphering Developmental Disorders Study, University of Washington Center for Mendelian Genomics
المصدر: American journal of human genetics [Am J Hum Genet] 2020 Jan 02; Vol. 106 (1), pp. 137. Date of Electronic Publication: 2019 Dec 24.
نوع المنشور: Published Erratum
اللغة: English
بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: PubMed not MEDLINE; MEDLINE
أسماء مطبوعة: Publication: 2008- : [Cambridge, MA] : Cell Press
Original Publication: Baltimore, American Society of Human Genetics.
التعليقات: Erratum for: Am J Hum Genet. 2019 Feb 7;104(2):319-330. (PMID: 30639322)
تواريخ الأحداث: Date Created: 20191228 Latest Revision: 20200825
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC7042478
DOI: 10.1016/j.ajhg.2019.11.014
PMID: 31879022
قاعدة البيانات: MEDLINE
الوصف
تدمد:1537-6605
DOI:10.1016/j.ajhg.2019.11.014