Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease.

Pecci, Alessandro (author)

Panza, Emanuele (author)

Pujol-Moix, Núria (author)

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Klersy, Catherine (author)

Di Bari, Filomena (author)

Bozzi, Valeria (author)

Gresele, Paolo (author)

Lethagen, Stefan (author)

Fabris, Fabrizio (author)

Dufour, Carlo (author)

Granata, Antonio (author)

Doubek, Michael (author)

Pecoraro, Carmine (author)

Koivisto, Pasi A (author)

Umeå universitet,Medicinsk och klinisk genetik

Heller, Paula G (author)

Iolascon, Achille (author)

Alvisi, Patrizia (author)

Schwabe, Dirk (author)

De Candia, Erica (author)

Rocca, Bianca (author)

Russo, Umberto (author)

Ramenghi, Ugo (author)

Noris, Patrizia (author)

Seri, Marco (author)

Balduini, Carlo L (author)

Savoia, Anna (author)

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 (creator_code:org_t)

2008

2008

English.

In: Hum Mutat. - 1098-1004. ; 29:3, s. 409-417

Related links:

http://www.ncbi.nlm....

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https://urn.kb.se/re...

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• Journal article (peer-reviewed)