The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

Eng, C (author)

Clayton, D (author)

Schuffenecker, I (author)

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Lenoir, G (author)

Cote, G (author)

Gagel, RF (author)

vanAmstel, HKP (author)

Lips, CJM (author)

Nishisho, I (author)

Takai, SI (author)

Marsh, DJ (author)

Robinson, BG (author)

FrankRaue, K (author)

Raue, F (author)

Xue, FY (author)

Noll, WW (author)

Romei, C (author)

Pacini, F (author)

Fink, M (author)

Niederle, B (author)

Zedenius, J (author)

Karolinska Institutet

Nordenskjold, M (author)

Karolinska Institutet

Komminoth, P (author)

Hendy, GN (author)

Gharib, H (author)

Thibodeau, SN (author)

Lacroix, A (author)

Frilling, A (author)

Ponder, BAJ (author)

Mulligan, LM (author)

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 (creator_code:org_t)

American Medical Association (AMA), 1996

1996

English.

In: JAMA. - : American Medical Association (AMA). - 0098-7484. ; 276:19, s. 1575-1579

Related links:

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• Journal article (peer-reviewed)