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Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia ( SPG42 ) caused by SLC33A1 mutation in a Chinese kindred
Author(s) -
Lin Pengfei,
Mao Fei,
Liu Qiji,
Shao Changshun,
Yan Chuanzhu,
Gong Yaoqin
Publication year - 2010
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.2485
Subject(s) - christian ministry , medicine , teratology , medical genetics , china , hereditary spastic paraplegia , family medicine , library science , genetics , pregnancy , biology , political science , phenotype , fetus , law , gene , computer science
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