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A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome
A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome
2020
Abdulsamad Wafa
Faten Moassass
Suher Almedani
Thomas Liehr
Kathleen Wilhelm
Manar As'sad
Sarah Knippenberg
Ralf Glaubitz
Rami A. Jarjour
Walid Al Achkar
Amedes Genetics
Keywords:
chd7 gene
Exon
Kallmann syndrome
Genetics
Biology
Correction
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