Molecular Analysis of Libyan Families with Allgrove Syndrome: Geographic Expansion of the Ancestral Mutation c.1331+1G>A in North Africa.

Fakhri Kallabi,Imen Ben Rebeh,Rahma Felhi,Dorra Sellami,Saber Masmoudi,Leila Keskes,Hassen Kamoun

Molecular Analysis of Libyan Families with Allgrove Syndrome: Geographic Expansion of the Ancestral Mutation c.1331+1G>A in North Africa.

2016

Fakhri Kallabi
Imen Ben Rebeh
Rahma Felhi
Dorra Sellami
Saber Masmoudi
Leila Keskes
Hassen Kamoun

Background/Aims: Allgrove syndrome is a rare autosomal recessive disorder characterized by alacrima, achalasia, and adrenal insufficiency. It is caused by mutatio

Keywords:

Alacrima
Achalasia
Adrenal insufficiency
Medicine
Allgrove Syndrome
Dominance (genetics)
Founder effect
Genetics
Point mutation
Mutation
molecular analysis
north africa
Biology

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