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Seco et al., 2015 - Google Patents

Allelic mutations of KITLG, encoding KIT ligand, cause asymmetric and unilateral hearing loss and Waardenburg syndrome type 2

Seco et al., 2015

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Document ID
16044111774900917536
Author
Seco C
de Castro L
Van Nierop J
Morín M
Jhangiani S
Verver E
Schraders M
Maiwald N
Wesdorp M
Venselaar H
Spruijt L
Oostrik J
Schoots J
van Reeuwijk J
Lelieveld S
Huygen P
Insenser M
Admiraal R
Pennings R
Hoefsloot L
Arias-Vásquez A
de Ligt J
Yntema H
Jansen J
Muzny D
Huls G
van Rossum M
Lupski J
Moreno-Pelayo M
Kunst H
Kremer H
Publication year
Publication venue
The American Journal of Human Genetics

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Snippet

Linkage analysis combined with whole-exome sequencing in a large family with congenital and stable non-syndromic unilateral and asymmetric hearing loss (NS-UHL/AHL) revealed a heterozygous truncating mutation, c. 286_303delinsT (p. Ser96Ter), in KITLG. This mutation …
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    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
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