Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation

Clinical Genetics

Volumn 57, Issue 3, 2000, Pages 232-234

  Pampanos, A ^a   Neou, P ^a   Iliades, T ^a   Apostolopoulos, N ^a   Voyiatzis, N ^a   Grigoriadou, M ^a   Katsichti, L ^a   Skevas, A ^a   Petersen, M B ^a  

^a AGHIA SOPHIA CHILDREN S HOSPITAL   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26;

CHROMOSOME 13Q; CONGENITAL DEAFNESS; DELETION MUTANT; DOMINANT INHERITANCE; FEMALE; HUMAN; LETTER; MALE; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

ALLELES; CONNEXINS; FAMILY HEALTH; FEMALE; GENE DELETION; GENES, DOMINANT; HEARING LOSS, SENSORINEURAL; HOMOZYGOTE; HUMANS; INFANT; MALE; PEDIGREE; POLYMERASE CHAIN REACTION;

EID: 0034069121     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2000.570311.x     Document Type: Letter

References (0)