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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and CHKB[original query]
TCRA, P2RY11, and CPT1B/CHKB associations in Chinese narcolepsy.
Sleep medicine 2012 Mar 13 (3): 269-72.
Han Fang, Lin Ling, Li Jing, Aran Adi, Dong Song X, An Pei, Zhao Long, Li Qian Y, Yan Han, Wang Jie S, Gao Hui Y, Li Mei, Gao Zhan C, Strohl Kingman P, Mignot Emmanu
A Rare Cause of Autism Spectrum Disorder: Megaconial Muscular Dystrophy.
Annals of Indian Academy of Neurology 2021 2 23 (5): 694-696.
Kutluk Gultekin, Kadem Naz, Bektas Omer, Eroglu Hatice N
Phenotype-genotype spectrum of a cohort of congenital muscular dystrophies: a single-centre experience from India.
Neurogenetics 2024 8 .
Tanushree Chawla, Saraswati Nashi, Dipti Baskar, Kiran Polavarapu, Seena Vengalil, Mainak Bardhan, Veeramani Preethish-Kumar, Ramya Sukrutha, Gopikrishnan Unnikrishnan, Akshata Huddar, Hansashree Padmanabha, Ram Murthy Anjanappa, Nandeesh Bevinahalli, Vidya Nittur, Manoj Rajanna, Gautham Arunachal Udupi, Atchayaram Nali
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