Erratum: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease (Nutrition and Metabolism)

Hyeon Jin Kim; Young Bin Hong; Jin Mo Park; Yu Ri Choi; Ye Jin Kim; Bo Ram Yoon; Heasoo Koo; Jeong Hyun Yoo; Sang Beom Kim; Minhwa Park; Ki Wha Chung; Byung Ok Choi

doi:10.1186/1750-1172-8-165

Erratum: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease (Nutrition and Metabolism)

Hyeon Jin Kim, Young Bin Hong, Jin Mo Park, Yu Ri Choi, Ye Jin Kim, Bo Ram Yoon, Heasoo Koo, Jeong Hyun Yoo, Sang Beom Kim, Minhwa Park, Ki Wha Chung, Byung Ok Choi

Department of Radiology

Research output: Contribution to journal › Comment/debate

3 Scopus citations

Original language	English
Article number	165
Journal	Orphanet Journal of Rare Diseases
Volume	8
Issue number	1
DOIs	https://doi.org/10.1186/1750-1172-8-165
State	Published - 2013

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10.1186/1750-1172-8-165

Cite this

Kim, H. J., Hong, Y. B., Park, J. M., Choi, Y. R., Kim, Y. J., Yoon, B. R., Koo, H., Yoo, J. H., Kim, S. B., Park, M., Chung, K. W., & Choi, B. O. (2013). Erratum: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease (Nutrition and Metabolism). Orphanet Journal of Rare Diseases, 8(1), Article 165. https://doi.org/10.1186/1750-1172-8-165

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author = "Kim, {Hyeon Jin} and Hong, {Young Bin} and Park, {Jin Mo} and Choi, {Yu Ri} and Kim, {Ye Jin} and Yoon, {Bo Ram} and Heasoo Koo and Yoo, {Jeong Hyun} and Kim, {Sang Beom} and Minhwa Park and Chung, {Ki Wha} and Choi, {Byung Ok}",

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T2 - Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease (Nutrition and Metabolism)

AU - Kim, Hyeon Jin

AU - Hong, Young Bin

AU - Park, Jin Mo

AU - Choi, Yu Ri

AU - Kim, Ye Jin

AU - Yoon, Bo Ram

AU - Koo, Heasoo

AU - Yoo, Jeong Hyun

AU - Kim, Sang Beom

AU - Park, Minhwa

AU - Chung, Ki Wha

AU - Choi, Byung Ok

PY - 2013

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DO - 10.1186/1750-1172-8-165

M3 - Comment/debate

C2 - 24228706

AN - SCOPUS:84887596394

SN - 1750-1172

VL - 8

JO - Orphanet Journal of Rare Diseases

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