Table of Contents

OpinionP:1-2

Modeling improvements for mitochondrial disease caused by mt-tRNA mutations: Patients' brain in a dish
Samantha Brooks*

DOI: 10.37532/ puljcgg.22.5 (1).1-2

• Abstract
• Full-Text
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OpinionP:1-2

Underlying variant roles in disease epidemiology: SARS-CoV-2 genomic variations from Gujarat
Lydia Hopkins*

DOI: 10.37532/puljcgg.22.5(1).1-2

• Abstract
• Full-Text
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OpinionP:1-2

The brugada syndrome is a rare arrhythmia disorder with complex inheritance
Genesis Stewart*

• Abstract
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CommentaryP:1-2

The function of mitochondria in autosomal-recessive optic atrophy
Brooklyn Warren*

• Abstract
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OpinionP:1-2

The olfactory receptor gene family's gender bias in copy number variation is influenced by ethnicity.
Elijah Mason*

DOI: 10.37532/puljcgg.22.5(1).1-2.

• Abstract
• Full-Text
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Original ArticleP:1-3

Molecular study of the ?-casein gene in water buffalo population of North-West of Iran
Masoumeh Firouzamandi*

• Abstract
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Case ReportsP:1-4

Non Random distribution of Chromosome -21 in Syndromic Cases of Wilms’ tumors
Ajit Kumar Saxena*, Vijayendra Kumar, Pritanjili Singh, Meenakshi Tiwari, Ramanuj K, Aprajita, Aniket K and Chandan K Singh

• Abstract
• Full-Text
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