TY  - GEN
AU  - Van Laer,L
AU  - Coucke,P
AU  - Mueller,R F
AU  - Caethoven,G
AU  - Flothmann,K
AU  - Prasad,S D
AU  - Chamberlin,G P
AU  - Houseman,M
AU  - Taylor,G R
AU  - Van de Heyning,C M
AU  - Fransen,E
AU  - Rowland,J
AU  - Cucci,R A
AU  - Smith,R J
AU  - Van Camp,G
TI  - A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment
SN  - 1468-6244
PY  - 2001///1205
KW  - Alleles
KW  - Connexin 26
KW  - Connexins
KW  - genetics
KW  - DNA
KW  - chemistry
KW  - DNA Mutational Analysis
KW  - Founder Effect
KW  - Gene Frequency
KW  - Genotype
KW  - Hearing Loss, Sensorineural
KW  - Humans
KW  - Mutation
KW  - Polymorphism, Single Nucleotide
KW  - Sequence Deletion
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1136/jmg.38.8.515
ER  -