Identification of the PLA2G6 c.1579G>A Missense Mutation in Papillon Dog Neuroaxonal Dystrophy Using Whole Exome Sequencing Analysis.

Tsuboi M, Watanabe M, Nibe K, Yoshimi N, Kato A, Sakaguchi M, Yamato O, Tanaka M, Kuwamura M, Kushida K, Ishikura T, Harada T, Chambers JK, Sugano S, Uchida K, Nakayama H. Identification of the PLA2G6 c.1579G>A Missense Mutation in Papillon Dog Neuroaxonal Dystrophy Using Whole Exome Sequencing Analysis. PLoS One. 2017; 12(1):e0169002.

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subject areas

Amino Acid Sequence
Animals
Dog Diseases
Dogs
Female
Group VI Phospholipases A2
Immunohistochemistry
Male
Mutation, Missense
Neuroaxonal Dystrophies
Pedigree
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger
Sequence Homology, Amino Acid

authors with profiles

James Chambers

RCMI CC is supported by the National Institute on Minority Health and Health Disparities, National Institutes of Health (NIH), through Grant Number U24MD015970. The contents of this site are solely the responsibility of the authors and do not necessarily represent the official views of the NIH

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