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P1148A in fibrillin‐1 is not a mutation leading to Shprintzen‐Goldberg syndrome
Author(s) -
Watanabe Yoriko,
Yano Shoji,
Koga Yasutoshi,
Yukizane Shigenori,
Nishiyori Atsushi,
Yoshino Makoto,
Kato Hirohisa,
Ogata Tsutomu,
Adachi Masanori
Publication year - 1997
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(1997)10:4<326::aid-humu10>3.0.co;2-1
Subject(s) - fibrillin , biology , genetics , mutation , gene