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 |