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Sheppard Siegal Syndrome (Familial Mediterranean Fever) With Homozygous M694v Gene Mutation and Saa1 Amyloidosis Gene Genotype 1.1/1.5: Documenting the Occurrence in An Iraqi Girl, And an Evidence-Based Therapeutic Recommendation
Citation
Aamir Jalal Al-Mosawi
Aamir Jalal Al-Mosawi (2022) Sheppard Siegal syndrome (Familial Mediterranean fever) with homozygous M694V gene mutation and SAA1 amyloidosis gene genotype 1.1/1.5: Documenting the occurrence in an Iraqi girl, and an evidence-based therapeutic recommendation. International Journal of Endocrinology Research and Reviews 2(1) : 01-04.