Maternally inherited cardiomyopathy: An atypical presentation of the mtDNA 12S rRNA gene A1555G mutation [3]

F. M. Santorelli; K. Tanji; P. Manta; C. Casali; S. Krishna; A. P. Hays; D. M. Mancini; S. DiMauro; M. Hirano

doi:10.1086/302188

Maternally inherited cardiomyopathy: An atypical presentation of the mtDNA 12S rRNA gene A1555G mutation [3]

F. M. Santorelli, K. Tanji, P. Manta, C. Casali, S. Krishna, A. P. Hays, D. M. Mancini, S. DiMauro, M. Hirano

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

96 Scopus citations

Original language	English
Pages (from-to)	295-300
Number of pages	6
Journal	American Journal of Human Genetics
Volume	64
Issue number	1
DOIs	https://doi.org/10.1086/302188
State	Published - 1999
Externally published	Yes

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10.1086/302188

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@article{1ce3a3e85ec942f3a22386bfc30c2b5f,

title = "Maternally inherited cardiomyopathy: An atypical presentation of the mtDNA 12S rRNA gene A1555G mutation [3]",

author = "Santorelli, \{F. M.\} and K. Tanji and P. Manta and C. Casali and S. Krishna and Hays, \{A. P.\} and Mancini, \{D. M.\} and S. DiMauro and M. Hirano",

note = "Funding Information: We thank Dr. Eduardo Bonilla for critical comments. This work was partially supported by National Institute of Child Health and Human Development program project PO1 HD32062, Telethon-Italy grant 844-1996 (to C.C.), Italian Ministry of Health grant 97/02/G/009 (to F.M.S.), and by grants from the Muscular Dystrophy Association. M.H. is supported by National Institutes of Health grant 1RO1 HL59657 and by the Columbia-Presbyterian Medical Center Irving Scholar program.",

year = "1999",

doi = "10.1086/302188",

language = "English",

volume = "64",

pages = "295--300",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "1",

}

TY - JOUR

T1 - Maternally inherited cardiomyopathy

T2 - An atypical presentation of the mtDNA 12S rRNA gene A1555G mutation [3]

AU - Santorelli, F. M.

AU - Tanji, K.

AU - Manta, P.

AU - Casali, C.

AU - Krishna, S.

AU - Hays, A. P.

AU - Mancini, D. M.

AU - DiMauro, S.

AU - Hirano, M.

N1 - Funding Information: We thank Dr. Eduardo Bonilla for critical comments. This work was partially supported by National Institute of Child Health and Human Development program project PO1 HD32062, Telethon-Italy grant 844-1996 (to C.C.), Italian Ministry of Health grant 97/02/G/009 (to F.M.S.), and by grants from the Muscular Dystrophy Association. M.H. is supported by National Institutes of Health grant 1RO1 HL59657 and by the Columbia-Presbyterian Medical Center Irving Scholar program.

PY - 1999

Y1 - 1999

UR - https://www.scopus.com/pages/publications/0033366515

U2 - 10.1086/302188

DO - 10.1086/302188

M3 - Letter

C2 - 9915970

AN - SCOPUS:0033366515

SN - 0002-9297

VL - 64

SP - 295

EP - 300

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 1

ER -