Prenatal diagnosis of autosomal dominant hereditary spastic...

Prenatal Diagnosis 2010 Vol. 30; Iss. 5

Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG42) caused by SLC33A1 mutation in a Chinese kindred

Pengfei Lin, Fei Mao, Qiji Liu, Changshun Shao, Chuanzhu Yan, Yaoqin Gong
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Volume:
30
Year:
2010
Language:
english
Pages:
1
DOI:
10.1002/pd.2485
File:
PDF, 151 KB
english, 2010
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