Lipoamide dehydrogenase deficiency in ashkenazi jews: An insertion mutation in the mitochondrial leader sequence

Orly N. Elpeleg; Avraham Shaag; Joseph Z. Glustein; Yair Anikster; Adina Joseph; Ann Saada

doi:10.1002/(SICI)1098-1004(1997)10:3<256::AID-HUMU16>3.0.CO;2-Z

Lipoamide dehydrogenase deficiency in ashkenazi jews: An insertion mutation in the mitochondrial leader sequence

Orly N. Elpeleg, Avraham Shaag, Joseph Z. Glustein, Yair Anikster, Adina Joseph, Ann Saada

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

Original language	English
Pages (from-to)	256-257
Number of pages	2
Journal	Human Mutation
Volume	10
Issue number	3
DOIs	https://doi.org/10.1002/(SICI)1098-1004(1997)10:3<256::AID-HUMU16>3.0.CO;2-Z
State	Published - 1997
Externally published	Yes

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10.1002/(SICI)1098-1004(1997)10:3<256::AID-HUMU16>3.0.CO;2-Z

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title = "Lipoamide dehydrogenase deficiency in ashkenazi jews: An insertion mutation in the mitochondrial leader sequence",

author = "Elpeleg, {Orly N.} and Avraham Shaag and Glustein, {Joseph Z.} and Yair Anikster and Adina Joseph and Ann Saada",

year = "1997",

doi = "10.1002/(SICI)1098-1004(1997)10:3<256::AID-HUMU16>3.0.CO;2-Z",

language = "אנגלית",

volume = "10",

pages = "256--257",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "Wiley-Liss Inc.",

number = "3",

}

TY - JOUR

T1 - Lipoamide dehydrogenase deficiency in ashkenazi jews

T2 - An insertion mutation in the mitochondrial leader sequence

AU - Elpeleg, Orly N.

AU - Shaag, Avraham

AU - Glustein, Joseph Z.

AU - Anikster, Yair

AU - Joseph, Adina

AU - Saada, Ann

PY - 1997

Y1 - 1997

UR - http://www.scopus.com/inward/record.url?scp=0030769124&partnerID=8YFLogxK

U2 - 10.1002/(SICI)1098-1004(1997)10:3<256::AID-HUMU16>3.0.CO;2-Z

DO - 10.1002/(SICI)1098-1004(1997)10:3<256::AID-HUMU16>3.0.CO;2-Z

M3 - מאמר

C2 - 9298831

AN - SCOPUS:0030769124

VL - 10

SP - 256

EP - 257

JO - Human Mutation

JF - Human Mutation

SN - 1059-7794

IS - 3

ER -

Lipoamide dehydrogenase deficiency in ashkenazi jews: An insertion mutation in the mitochondrial leader sequence

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