Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Muscle Weakness and SMN1[original query] |
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[Molecular analysis of survival motor neuron gene in 338 suspicious children patients with spinal muscular atrophy]. Zhonghua er ke za zhi. Chinese journal of pediatrics 2008 Dec 46 (12): 919-23. Song Fang, Qu Yu-jin, Zou Li-ping, Wang Li-wen, Long Mei-juan, Wang Xu, Yang Yan-ling, Chen Qian, Wang Hong, Jin Yu-w |
Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran. Advanced biomedical research 2014 3 74. Sedghi Maryam, Behnam Mahdiyeh, Fazel Esmat, Salehi Mansoor, Ganji Hamid, Meamar Rokhsareh, Hosseinzadeh Majid, Nouri Nayer |
Frequency of SMN1 deletion carriers in a Mestizo population of central and northeastern Mexico: A pilot study. Experimental and therapeutic medicine 2015 Jun 9 (6): 2053-2058. Contreras-Capetillo Silvina Noemi, Blanco Hugo Leonid Gallardo, Cerda-Flores Ricardo Martin, Lugo-Trampe José, Torres-Muñoz Iris, Bravo-Oro Antonio, Esmer Carmen, DE Villarreal Laura Ella Martín |
Genetic findings of Cypriot spinal muscular atrophy patients. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Oct 36 (10): 1829-34. Theodorou L, Nicolaou P, Koutsou P, Georghiou A, Anastasiadou V, Tanteles G, Kyriakides T, Zamba-Papanicolaou E, Christodoulou |
Genotype-Phenotype Correlation of SMN1 and NAIP Deletions in Korean Patients with Spinal Muscular Atrophy. Journal of clinical neurology (Seoul, Korea) 2016 Oct . Ahn Eun Ji, Yum Mi Sun, Kim Eun Hee, Yoo Han Wook, Lee Beom Hee, Kim Gu Hwan, Ko Tae Su |
Carrier frequency of spinal muscular atrophy in Thailand. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 Apr . Dejsuphong Donniphat, Taweewongsounton Aruchalean, Khemthong Pollawat, Chitphuk Sermsiri, Stitchantrakul Wasana, Sritara Piyamitr, Tunteeratum Atchara, Sura Thanyach |
Phenotypes of SMA patients retaining SMN1 with intragenic mutation. Brain & development 2021 4 43 (7): 745-758. Wijaya Yogik Onky Silvana, Ar Rohmah Mawaddah, Niba Emma Tabe Eko, Morisada Naoya, Noguchi Yoriko, Hidaka Yasufumi, Ozasa Shiro, Inoue Takeshi, Shimazu Tomoyuki, Takahashi Yuya, Tozawa Takenori, Chiyonobu Tomohiro, Inoue Takushi, Shiroshita Tomoyoshi, Yokoyama Atsushi, Okamoto Kentaro, Awano Hiroyuki, Takeshima Yasuhiro, Saito Toshio, Saito Kayoko, Nishio Hisahide, Shinohara Masaka |
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- Page last updated:Apr 29, 2024
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