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Journal of Genetic Mutation Disorders
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Volume 1 · Issue 1 · 2025
7 articles in this issue
JGMD
#1
Spinal Muscular Atrophy-Type1, Unraveling the tapestry from highly inbred region of North India
Dil-Afroze
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JGMD
#2
E. Coli Bacteria and It's Transcription Regulation
Bhattacharya PK
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JGMD
#3
A Novel Hemizygous Mutation of HCFC1 Causes X-Linked Recessive Gene Inherited Developmental Delay in a Chinese Family
Chen J
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JGMD
#4
A Novel Coenzyme Q8A Mutation in a Case with Juvenile-Onset Coenzyme Q10D4: Case Report and Literature Review
Dedeoğlu O
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JGMD
#5
Sequence Variant in the TRIM39-RPP21 Gene Readthrough is Shared Across a Cohort of Arabian Foals Diagnosed with Juvenile Idiopathic Epilepsy
Polani S
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JGMD
#6
Two Novel Cases of Marfan Syndrome with FBN1 whole Gene Deletion: Laboratory Assay and Cases Review
Spitalieri P
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JGMD
#7
Mthfr c677t, Homocysteine and Risk of Splanchnic Vein Thrombosis: A Pooled Analysis of Published Epidemiological Studies
Li SL
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