A <i>de novo</i> Mutation (p.Gln277X) of <i>Cyclin D2</i> is Responsible for a Child with Megalencephaly–Polymicrogyria–Polydactyly–Hydrocephalus Syndrome-Reference-Cited by-同舟云学术

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A de novo Mutation (p.Gln277X) of Cyclin D2 is Responsible for a Child with Megalencephaly–Polymicrogyria–Polydactyly–Hydrocephalus Syndrome

Published:2024-07-01 Issue:7 Volume:43 Page:325-330
ISSN:1044-5498
Container-title:DNA and Cell Biology
language:en
Short-container-title:DNA and Cell Biology

Author:

Zhao Mei-Fang¹^ORCID,Zhang Song-Lin²,Xiang YangZiYu¹,Wang Qian¹,Cao Gao-Hui¹,Zhang Ping-Ping³,Fan Liang-Liang¹^ORCID,Yu Rong⁴,Li Ya-Li³

Affiliation:

1. Department of Cell Biology, School of Life Sciences, Central South University, Changsha, Republic of China.

2. Peking University China-Japan Friendship School of Clinical Medicine, Beijing, Republic of China.

3. Departments of Reproductive Genetics, HeBei General Hospital, Shijiazhuang, Republic of China.

4. Department of Anesthesiology, The Second Xiangya Hospital, Central South University, Changsha, Republic of China.

Publisher

Mary Ann Liebert Inc

Link

https://www.liebertpub.com/doi/pdf/10.1089/dna.2023.0391

Reference17 articles.

1. Gene identification and functional analysis of a D-type cyclin (CCND2) in freshwater pearl mussel (Hyriopsis cumingii)

2. Medulloblastoma in the setting of megalencephaly polymicrogyria polydactyly hydrocephalus

3. CCND2 mutations in atypical chronic myeloid leukemia: a report of two cases

4. Restoration of cyclin D2 has an inhibitory potential on the proliferation of LNCaP cells

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