Novel mutation in two brothers with Hermansky Pudlak syndrome type 3

K Sandrock-Lang, I Bartsch, N Buechele… - Blood Cells, Molecules …, 2017 - Elsevier
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder causing
oculocutaneous albinism, bleeding disorder and ceroid lipofuscinosis. Platelets from HPS …
被引用次数：13 相关文章

Novel mutation in two brothers with Hermansky Pudlak syndrome type 3

K Sandrock-Lang, I Bartsch… - … cells, molecules & …, 2017 - pubmed.ncbi.nlm.nih.gov
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder causing
oculocutaneous albinism, bleeding disorder and ceroid lipofuscinosis. Platelets from HPS …

Novel mutation in two brothers with Hermansky Pudlak syndrome type 3.

K Sandrock-Lang, I Bartsch, N Buechele… - … Cells, Molecules & …, 2017 - europepmc.org
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder causing
oculocutaneous albinism, bleeding disorder and ceroid lipofuscinosis. Platelets from HPS …

[引用][C] Novel mutation in two brothers with Hermansky Pudlak syndrome type 3

K Sandrock-Lang, I Bartsch, N Buechele… - Blood Cells, Molecules …, 2017 - cir.nii.ac.jp
Novel mutation in two brothers with Hermansky Pudlak syndrome type 3 | CiNii Research CiNii
国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォームへ移動 論文・データを …