Additive dominant effect of a SOX10 mutation underlies a complex phenotype of PCWH.

scientific article published on 7 May 2015

Additive dominant effect of a SOX10 mutation underlies a complex phenotype of PCWH. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.NBD.2015.04.013
P698PubMed publication ID25959061

P2093author name stringKen Inoue
Shinichi Kohsaka
Chihiro Akazawa
Takayoshi Inoue
Yukiko U Inoue
Masumi Inagaki
Yukiko Ito
Yoshiki Matsuda
Naoko Inoue
Shoko Nakamura
Junko Asami
Yu-ichi Goto
Takahiro Ohkubo
Youhei W Terakawa
P304page(s)1-14
P577publication date2015-05-07
P1433published inNeurobiology of DiseaseQ15716606
P1476titleAdditive dominant effect of a SOX10 mutation underlies a complex phenotype of PCWH.
P478volume80

Reverse relations

cites work (P2860)
Q5278047122q11.2q13 duplication including SOX10 causes sex-reversal and peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease.
Q37159877Brain enhancer activities at the gene-poor 5p14.1 autism-associated locus
Q47904370Transcription factor Sox10 regulates oligodendroglial Sox9 levels via microRNAs
Q53267844Waardenburg syndrome: a rare cause of inherited neuropathy due to SOX10 mutation.

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