J. Willard Marriott Digital Library

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	Title	Date	Type	Setname
1	A Novel De Novo KIF21A Variant in a Patient With Congenital Fibrosis of the Extraocular Muscles With a Syndromic CFEOM Phenotype	2021-03	Text	ehsl_novel_jno
2	A Rare Mutation Associated With Probable Late-Onset Leber's Hereditary Optic Neuropathy	2020-09	Text	ehsl_novel_jno
3	Acetazolamide-Induced Nephrolithiasis in Idiopathic Intracranial Hypertension Patients	2016-06	Text	ehsl_novel_jno
4	The ACT3 gene and epigenetics	1997-08	Text	ir_etd
5	Clinical Features of Chinese Sporadic Leber Hereditary Optic Neuropathy Caused by Rare Primary mtDNA Mutations	2020-03	Text	ehsl_novel_jno
6	Clinical Features of Chinese Sporadic Leber Hereditary Optic Neuropathy Caused by Rare Primary mtDNA Mutations	2020-03	Text	ehsl_novel_jno
7	Combined Optic Atrophy and Rod-Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype	2021-09	Text	ehsl_novel_jno
8	Conversion to Leber Hereditary Optic Neuropathy After Hyperbaric Oxygen Therapy	2023-09	Text	ehsl_novel_jno
9	Cuban Epidemic Optic Neuropathy	1996-09	Text	ehsl_novel_jno
10	Diversification of Hox gene function as a consequence of evolution in cis-regulator sequences.	2001-05	Text	ir_etd
11	Evaluation of Vision-Related Quality of Life in Chinese Patients With Leber Hereditary Optic Neuropathy and the G11778A Mutation.	2019-03	Text	ehsl_novel_jno
12	The Genetic Testing Paradigm for Leber's Hereditary Optic Neuropathy: Discovery of a New Candidate LHON Mitochondrial DNA Mutation	2004-03-31	Text	ehsl_novel_nam
13	Homeotic genes and regional specification in Drosophila: characterization of the abdominalA gene and mechanisms of transcriptional control by homeotic proteins	1993-06	Text	ir_etd
14	Horizontal Gaze Palsy and Progressive Scoliosis With ROBO 3 Mutations in Patients From Cape Verde	2017-06	Text	ehsl_novel_jno
15	Infantile Presentation of Leber Hereditary Optic Neuropathy 'Plus' Disease	2019-06	Text	ehsl_novel_jno
16	Interaction of DNA-binding protein H-NS with the flagellar motor of E. coli	2013-12	Text	ir_etd
17	Leber Hereditary Optic Neuropathy in a Family of Carriers of MT-ND5 m.13042G>T (A236S) Novel Variant	2023-09	Text	ehsl_novel_jno
18	Leber Hereditary Optic Neuropathy in a Mother and Daughter Associated With m.10197G>A Mutation	2019-03	Text	ehsl_novel_jno
19	Lethal mutations in the isoprenoid pathway of salmonella enterica	2006	Text	ir_uspace
20	Modeling the amplification dynamics of human Alu retrotransposons	2005	Text	ir_uspace
21	Multilocus Mitochondrial Mutations Do Not Directly Affect the Efficacy of Gene Therapy for Leber Hereditary Optic Neuropathy	2020-03	Text	ehsl_novel_jno
22	Multilocus Mitochondrial Mutations Do Not Directly Affect the Efficacy of Gene Therapy for Leber Hereditary Optic Neuropathy	2020-03	Text	ehsl_novel_jno
23	Novel Mitochondrial Translation Optimizer-1 Mutations as a Cause of Hereditary Optic Neuropathy	2020-09	Text	ehsl_novel_jno
24	Novel Mutations of mtDNA m.14568G>A/m.14568C>T in MT-ND6 and m.7299A>G in MT-CO1: Evidence of Pathogenicity in Leber Hereditary Optic Neuropathy	2020-12	Text	ehsl_novel_jno
25	Optic Nerve Involvement in Farber Lipogranulomatosis: Expanding the Phenotypic Spectrum	2019-09	Text	ehsl_novel_jno

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