Complete Deficiency of Plasma Lecithin-Cholesterol Acyltransferase (LCAT) Activity Due to a Novel Homozygous Mutation (Gly-30-Ser) in the LCAT Gene

J.S. Owen; H. Wiebusch; P. Cullen; Gerald Watts; V.L.M. Lima; H. Funke; G. Assmann

doi:10.1002/(SICI)1098-1004(1996)8:1<79::AID-HUMU13>3.0.CO;2-O

Complete Deficiency of Plasma Lecithin-Cholesterol Acyltransferase (LCAT) Activity Due to a Novel Homozygous Mutation (Gly-30-Ser) in the LCAT Gene

J.S. Owen, H. Wiebusch, P. Cullen, Gerald Watts, V.L.M. Lima, H. Funke, G. Assmann

Graduate Research School

Research output: Contribution to journal › Article › peer-review

12 Citations (Scopus)

Original language	English
Pages (from-to)	79-82
Journal	Human Mutation
Volume	8
Issue number	N/A
DOIs	https://doi.org/10.1002/(SICI)1098-1004(1996)8:1<79::AID-HUMU13>3.0.CO;2-O
Publication status	Published - 1996

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10.1002/(SICI)1098-1004(1996)8:1<79::AID-HUMU13>3.0.CO;2-O

Cite this

@article{e8b5003a0ded4bdf8ff55f5b14e7bb70,

title = "Complete Deficiency of Plasma Lecithin-Cholesterol Acyltransferase (LCAT) Activity Due to a Novel Homozygous Mutation (Gly-30-Ser) in the LCAT Gene",

author = "J.S. Owen and H. Wiebusch and P. Cullen and Gerald Watts and V.L.M. Lima and H. Funke and G. Assmann",

year = "1996",

doi = "10.1002/(SICI)1098-1004(1996)8:1<79::AID-HUMU13>3.0.CO;2-O",

language = "English",

volume = "8",

pages = "79--82",

journal = "Human Mutation",

publisher = "Wiley-Liss",

number = "N/A",

}

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T1 - Complete Deficiency of Plasma Lecithin-Cholesterol Acyltransferase (LCAT) Activity Due to a Novel Homozygous Mutation (Gly-30-Ser) in the LCAT Gene

AU - Owen, J.S.

AU - Wiebusch, H.

AU - Cullen, P.

AU - Watts, Gerald

AU - Lima, V.L.M.

AU - Funke, H.

AU - Assmann, G.

PY - 1996

Y1 - 1996

U2 - 10.1002/(SICI)1098-1004(1996)8:1<79::AID-HUMU13>3.0.CO;2-O

DO - 10.1002/(SICI)1098-1004(1996)8:1<79::AID-HUMU13>3.0.CO;2-O

M3 - Article

VL - 8

SP - 79

EP - 82

JO - Human Mutation

JF - Human Mutation

IS - N/A

ER -