Epistatic connections between microphthalmia‐associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders
K Sato‐Jin, EK Nishimura, E Akasaka… - The FASEB …, 2008 - Wiley Online Library
Waardenburg syndrome (WS) is an inherited sensorineural deafness condition in humans
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
[PDF][PDF] Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary …
K Sato-Jin, EK Nishimura, E Akasaka, W Huber… - Citeseer
Waardenburg syndrome (WS) is an inherited sensorineural deafness condition in humans
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders
K Sato-Jin, EK Nishimura, E Akasaka… - … publication of the …, 2008 - pubmed.ncbi.nlm.nih.gov
Waardenburg syndrome (WS) is an inherited sensorineural deafness condition in humans
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
[引用][C] Epistatic connections between microphthalmia‐associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary …
K Sato‐Jin, EK Nishimura, E Akasaka, W Huber… - The FASEB …, 2007 - cir.nii.ac.jp
Epistatic connections between microphthalmia‐associated transcription factor and
endothelin signaling in Waardenburg syndrome and other pigmentary disorders | CiNii …
endothelin signaling in Waardenburg syndrome and other pigmentary disorders | CiNii …
Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders.
K Sato-Jin, EK Nishimura, E Akasaka… - … : Official Publication of …, 2007 - europepmc.org
Waardenburg syndrome (WS) is an inherited sensorineural deafness condition in humans
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
[PDF][PDF] Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary …
K Sato-Jin, EK Nishimura, E Akasaka, W Huber… - researchgate.net
Waardenburg syndrome (WS) is an inherited sensorineural deafness condition in humans
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
[PDF][PDF] Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary …
K Sato-Jin, EK Nishimura, E Akasaka, W Huber… - academia.edu
Waardenburg syndrome (WS) is an inherited sensorineural deafness condition in humans
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
caused by melanocyte deficiencies in the inner ear and forelock. Mutation of microphthalmia …
[引用][C] Epostatic connections between microphthalmia-associated trancecription factor and endothelin signaling in Waardenburg syndrome and other pigmentary …
K Sato-Jin - kanazawa-u.repo.nii.ac.jp
[引用][C] Epostatic connections between microphthalmia-associated trancecription factor and endothelin signaling in Waardenburg syndrome and other pigmentary …
K Sato-Jin - kanazawa-u.repo.nii.ac.jp