Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss.

Yan, Denise

Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss. [electronic resource] - American journal of medical genetics. Part A Feb 2007 - 385-6 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural

1552-4825

10.1002/ajmg.a.31553 doi


Chromosomes, Human, Pair 13
Connexin 26
Connexins--genetics
Female
Gene Frequency
Hearing Loss--genetics
Homozygote
Humans
Male
Sequence Deletion
Uniparental Disomy