PMID- 10364543
OWN - NLM
STAT- MEDLINE
DCOM- 19990805
LR  - 20191210
IS  - 0002-9297 (Print)
IS  - 0002-9297 (Linking)
VI  - 65
IP  - 1
DP  - 1999 Jul
TI  - Possible interaction between USH1B and USH3 gene products as implied by apparent 
      digenic deafness inheritance.
PG  - 261-5
FAU - Adato, A
AU  - Adato A
FAU - Kalinski, H
AU  - Kalinski H
FAU - Weil, D
AU  - Weil D
FAU - Chaib, H
AU  - Chaib H
FAU - Korostishevsky, M
AU  - Korostishevsky M
FAU - Bonne-Tamir, B
AU  - Bonne-Tamir B
LA  - eng
PT  - Letter
PT  - Research Support, Non-U.S. Gov't
PL  - United States
TA  - Am J Hum Genet
JT  - American journal of human genetics
JID - 0370475
RN  - 0 (Genetic Markers)
RN  - 0 (MYO7A protein, human)
RN  - 0 (Myosin VIIa)
RN  - EC 3.6.4.1 (Myosins)
RN  - EC 3.6.4.2 (Dyneins)
SB  - IM
MH  - Dyneins
MH  - Female
MH  - Genes, Recessive
MH  - Genetic Markers
MH  - Hearing Loss, Sensorineural/*genetics
MH  - Humans
MH  - Male
MH  - Myosin VIIa
MH  - Myosins/*genetics/physiology
MH  - Pedigree
MH  - Polymorphism, Genetic
MH  - Syndrome
PMC - PMC1378101
EDAT- 1999/06/12 10:00
MHDA- 2000/03/21 09:00
CRDT- 1999/06/12 10:00
PHST- 1999/06/12 10:00 [pubmed]
PHST- 2000/03/21 09:00 [medline]
PHST- 1999/06/12 10:00 [entrez]
AID - S0002-9297(07)63753-7 [pii]
AID - 10.1086/302438 [doi]
PST - ppublish
SO  - Am J Hum Genet. 1999 Jul;65(1):261-5. doi: 10.1086/302438.