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A point mutation in codon 3 of connexin‐32 is associated with X‐linked charcot‐marie‐tooth neuropathy
Author(s) -
Gupta Sanjoy,
Benstead Timothy,
Neumann Paul,
Guernsey Duane
Publication year - 1996
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/(sici)1098-1004(1996)8:4<375::aid-humu14>3.0.co;2-#
Subject(s) - biology , point mutation , genetics , connexin , mutation , connexin 32 , tooth disease , gene , gap junction , intracellular