Letter to the Editor: Neuropathy, ataxia, retinitis pigmentosa-like phenotype associated with a mitochondrial G8363A mutation in a family

Soo Yeon Kim; Ji Yoon Han; Hyun Ah Kim; Byung Chan Lim; Ji Eun Seo; Murim Choi; Ki Joong Kim; In Goo Lee; Jong Hee Chae

Letter to the Editor: Neuropathy, ataxia, retinitis pigmentosa-like phenotype associated with a mitochondrial G8363A mutation in a family

Soo Yeon Kim, Ji Yoon Han, Hyun Ah Kim, Byung Chan Lim, Ji Eun Seo, Murim Choi, Ki Joong Kim, In Goo Lee, Jong Hee Chae

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	546-548
Number of pages	3
Journal	Annals of clinical and laboratory science
Volume	48
Issue number	4
State	Published - 1 Jul 2018

Bibliographical note

Funding Information:
We thank the patient and her family for providing informed consent to publish this report. This study was supported by a grant from the Korea Healthcare Technology R&D project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry for Health & Welfare, Republic of Korea (Grant No. HI12C0066).

Cite this

@article{2ac53bb62fb1485da1556da01ece2606,

title = "Letter to the Editor: Neuropathy, ataxia, retinitis pigmentosa-like phenotype associated with a mitochondrial G8363A mutation in a family",

author = "Kim, {Soo Yeon} and Han, {Ji Yoon} and Kim, {Hyun Ah} and Lim, {Byung Chan} and Seo, {Ji Eun} and Murim Choi and Kim, {Ki Joong} and Lee, {In Goo} and Chae, {Jong Hee}",

note = "Funding Information: We thank the patient and her family for providing informed consent to publish this report. This study was supported by a grant from the Korea Healthcare Technology R&D project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry for Health & Welfare, Republic of Korea (Grant No. HI12C0066).",

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pages = "546--548",

journal = "Annals of clinical and laboratory science",

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T1 - Letter to the Editor

T2 - Neuropathy, ataxia, retinitis pigmentosa-like phenotype associated with a mitochondrial G8363A mutation in a family

AU - Kim, Soo Yeon

AU - Han, Ji Yoon

AU - Kim, Hyun Ah

AU - Lim, Byung Chan

AU - Seo, Ji Eun

AU - Choi, Murim

AU - Kim, Ki Joong

AU - Lee, In Goo

AU - Chae, Jong Hee

N1 - Funding Information: We thank the patient and her family for providing informed consent to publish this report. This study was supported by a grant from the Korea Healthcare Technology R&D project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry for Health & Welfare, Republic of Korea (Grant No. HI12C0066).

PY - 2018/7/1

Y1 - 2018/7/1

UR - http://www.scopus.com/inward/record.url?scp=85052120453&partnerID=8YFLogxK

M3 - Letter

C2 - 30143501

AN - SCOPUS:85052120453

SN - 0091-7370

VL - 48

SP - 546

EP - 548

JO - Annals of clinical and laboratory science

JF - Annals of clinical and laboratory science

IS - 4

ER -

Letter to the Editor: Neuropathy, ataxia, retinitis pigmentosa-like phenotype associated with a mitochondrial G8363A mutation in a family

Bibliographical note

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