Basal ganglia calcification and novel compound heterozygous mutations in the PANK2 gene in a Chinese boy with classic Pantothenate kinase-associated neurodegeneration-Reference-Cited by-同舟云学术

Basal ganglia calcification and novel compound heterozygous mutations in the PANK2 gene in a Chinese boy with classic Pantothenate kinase-associated neurodegeneration

Published:2018-04 Issue:15 Volume:97 Page:e0316
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Shi Xulai,Zheng Feixia,Ye Xiuyun,Li Xiucui,Zhao Qianlei,Lin Zhongdong,Hu Ying,Wang Jiwen

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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3. Atypical pantothenate kinase-associated neurodegeneration: clinical description of two brothers and a review of the literature;Mahoui;Rev Neurol,2017

4. Consensus clinical management guideline for pantothenate kinase-associated neurodegeneration (PKAN);Hogarth;Mol Genet Metab,2017

5. Clinical and genetic features of PKAN patients in a tertiary centre in Turkey;Akcakaya;Clin Neurol Neurosurg,2017

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