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Academic Journal

Familial amyloid polyneuropathy with chronic paroxysmal dry cough in Mainland China: A Chinese family with a proven heterozygous missense mutation c.349G>T in the transthyretin gene.

  • Authors : Yuan Z; Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.; Guo L

Subjects: Amyloid Neuropathies, Familial/Amyloid Neuropathies, Familial/Amyloid Neuropathies, Familial/*genetics ; Cough/Cough/Cough/*genetics ; Prealbumin/Prealbumin/Prealbumin/*geneticsAmyloidosis, Hereditary, Transthyretin-Related

  • Source: Journal Of Clinical Neuroscience: Official Journal Of The Neurosurgical Society Of Australasia [J Clin Neurosci] 2019 Feb; Vol. 60, pp. 164-166. Date of Electronic Publication: Publisher: Churchill Livingstone Country of Publication: Scotland NLM ID: 9433352 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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