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Am J Hum Genet
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
- A.K. Arndt
- S. Schaefer
- J.D. Drenckhahn
- M.K. Sabeh
- E.R. Plovie
- A. Caliebe
- E. Klopocki
- G. Musso
- A.A. Werdich
- H. Kalwa
- M. Heinig
- R.F. Padera
- K. Wassilew
- J. Bluhm
- C. Harnack
- J. Martitz
- P.J. Barton
- M. Greutmann
- F. Berger
- N. Huebner
- R. Siebert
- H.H. Kramer
- S.A. Cook
- C.A. Macrae
- S. Klaassen