Literature DB >> 33380712

Authors' response.

S Danda1, B M Thomas1, G Paramshivam1, Raji Thomas2, John Mathew3, D Danda3.   

Abstract

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Year:  2020        PMID： 33380712      PMCID： PMC8061587          DOI： 10.4103/0971-5916.305172

Source DB:  PubMed          Journal:  Indian J Med Res        ISSN： 0971-5916            Impact factor:   2.375


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  3 in total

1.  Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy.

Authors:  Yanchun Ji; Min Liang; Juanjuan Zhang; Ling Zhu; Zengjun Zhang; Runing Fu; Xiaoling Liu; Minglian Zhang; Qun Fu; Fuxin Zhao; Yi Tong; Yanhong Sun; Pingping Jiang; Min-Xin Guan
Journal:  Invest Ophthalmol Vis Sci       Date:  2016-05-01       Impact factor: 4.799

2.  Unmasking fibromyalgia as a mitochondrial disorder requires search for more than a single variant or single mtDNA deletions.

Authors:  Josef Finsterer
Journal:  Indian J Med Res       Date:  2020-10       Impact factor: 2.375

3.  Next-generation sequencing identifies novel mitochondrial variants in pituitary adenomas.

Authors:  K Németh; O Darvasi; I Likó; N Szücs; S Czirják; L Reiniger; B Szabó; P A Kurucz; L Krokker; P Igaz; A Patócs; H Butz
Journal:  J Endocrinol Invest       Date:  2019-01-25       Impact factor: 4.256
  3 in total

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