Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation

Eitemau Tebyg

• Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation
  gan: Shweta Birla, et al.
  Cyhoeddwyd: (2014-01-01)
• Multiple endocrine neoplasia type 2A with cutaneous lichen amyloidosis
  gan: Malhotra, Rakhi, et al.
  Cyhoeddwyd: (2020)
• Rare association of acromegaly with left atrial myxoma in Carney's complex due to novel PRKAR1A mutation
  gan: Birla, Shweta, et al.
  Cyhoeddwyd: (2014)
• The RET C611Y mutation causes MEN 2A and associated cutaneous lichen amyloidosis
  gan: Qi, Xiao-Ping, et al.
  Cyhoeddwyd: (2018)
• Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis
  gan: Hansford, J., et al.
  Cyhoeddwyd: (2000)